News

February 25, 2010 —  Medical device manufacturer Guidant LLC, a wholly owned subsidiary of Boston Scientific Corporation, was charged today with criminal violations of the Federal Food, Drug, and...

February 25, 2010 — A case-based interactive symposium will explore clinical correlations and controversies in the area of atrial fibrillation.

February 22, 2010 – The session “The Future is Now: Changing Paradigms in Atrial Fibrillation (AF) Management,” will take place 8 a.m. to noon Saturday, March 13 in Atlanta, Ga., in room A301,...

At ACC 2010, Philips Healthcare will focus on the full spectrum of cardiology care – from diagnosis and treatment to disease management and home monitoring to enhance patient care.

February 8, 2010 – Partnering with leading implantable cardioverter defibrillators (ICD) and pacemaker manufacturers, ScottCare Corp. has consolidated device information into one common platform...

February 8, 2010 – The FDA cleared the Sorin Paradym CRT Model 8750, a cardiac resynchronization therapy defibrillator (CRT-D), which features a new battery technology that delivers 37 joules, one...

February 5, 2010 – European CE mark approval was granted and first implants reported for the Fortify and Fortify ST implantable cardioverter defibrillators (ICD) and Unify cardiac...

February 5, 2010 – Cardiac surgical ablation system maker AtriCure agreed to pay $3.8 million plus interest for allegedly using illegal kickbacks and an off-label marketing campaign to induce...

February 3, 2010 – The new Gator ClipSeal Plug is designed to maintain a hemostatic seal around 0.035- or 0.038-inch guide wires within large hemostatic valve introducer sheaths to minimize blood...

February 3, 2010 – Results of a four-year study evaluating the safety and efficacy of laser assisted lead removal using the Spectranetics laser sheath (SLS II), found a 97.7 percent clinical...

February 2, 2010 - A second-generation transradial compression bracelet, the Zoom 2010, is being released by Zoom Co Medic. This bracelet is designed to obtain a stable compression of the radial...

January 26, 2010 — According to data appearing today in JAMA , patients with atrial fibrillation, a common heart rhythm disorder, who were treated with catheter ablation using the NaviStar...

January 18, 2010 – A 10-year follow-up of patients with implantable cardioverter defibrillators (ICDs) will determine long-term outcomes of ICD therapy in heart failure patients.

January 15, 2010 – A large-capacity radio frequency identification (RFID) enabled cabinet has been introduced for operating room supply centers and catheterization labs.

January 15, 2010 – The U.S. Patent Office this week issued a patent for the wireless transmission system used by the CardioBip remote monitor, which generates recordings equivalent in quality with...

January 2, 2010 – The FDA cleared the Celsius RMT ThermoCool ablation catheter for use with Stereotaxis' magnetic navigation system in the treatment of type 1 atrial flutter.

January 6, 2010 – The FDA, in collaboration with major implantable pacemaker and implantable cardioverter-defibrillator (ICD) manufacturers, demonstrated the effects of emissions from radio...

January 4, 2010 – The new design of the D-Stat Rad-Band incorporates a quick-release feature and a larger release tab, making it easier to detach the translucent comfort pad without disrupting...

December 24, 2009 – The U.S. Department of Justice and Boston Scientific Corp. yesterday entered into a civil settlement regarding an investigation of post-market surveys conducted by Guidant Corp...

December 14, 2009 – First new anti-arrhythmic drug to be approved in the European Union in the last 10 years was recently granted European Commission marketing authorization.

December 9, 2009 — A feasibility clinical trial was launched last week to evaluate the safety and efficacy of a combined surgical and catheter procedure, the convergent procedure, for the...

December 8, 2009 – The U.S. Food and Drug Administration (FDA) gave 510(k) clearance last week for Spectranetics’ new VisiSheath Dilator Sheath for pacing and defibrillator lead removal. The...

December 7, 2009 - A new integrated hybrid interventional table offers head-to-toe tilting and side-to-side cradling to meet the needs of both interventionalists and surgeons during hybrid...

December 4, 2009 – In an effort to lower clinician radiation exposure in the cath lab, a new device displays the real-time dose each clinician receives and alerts them when they enter the...

November 18, 2009 – The Journal of Cardiac Failure published results from a study showing ventilatory expired gas analysis during a short bout of low-intensity exercise may provide insight into...

November 12, 2009 – The first enrollments were made this week in the global Attain Success trial that will evaluate implant success, complication rates and procedure times in the market-released...

The incidence of cardiac arrhythmia is expected to increase significantly with an aging U.S. population and rising rates of obesity. In 2008, atrial fibrillation (AF), the most common complex...

November 9, 2009 – Boston Scientific Corp. today announced the launch of its COGNIS cardiac resynchronization therapy defibrillator (CRT-D) and the TELIGEN implantable cardioverter defibrillator (...

November 9, 2009 – Boston Scientific Corp. said Friday it reached an agreement in principle with the U.S. Department of Justice (DOJ) related to product advisories issued by its Guidant subsidiary...

November 6, 2009 — Stereotaxis received notice this week that its Celsius RMT ThermoCool catheter received CE mark for distribution in the European market.

November 4, 2009 — BIOTRONIK Inc. this week announced the results from site preparation, antibiotic use and infection sub-analysis from the REPLACE Registry.

November 6, 2009 – Nearly 4 million people nationwide suffer from cardiac arrhythmias each year, according to the 2006 U.S. Cardiac Rhythm Management Market report by Frost and Sullivan. About 2.5...

November 3, 3009 — On Monday, Andrea Natale, M.D., FACC, FHRS, an electrophysiologist and executive medical director of the Texas Cardiac Arrhythmia Institute at St. David's Medical Center, became...

November 2, 2009 — Ascent Healthcare Solutions said last week it received the industry’s first and only 510(k) clearance from the U.S. Food and Drug Administration to reprocess the Biosense...

October 27, 2009 – Defibtech and Cintas Corp. will introduce the new ReviveR View automated external defibrillator (AED), which features a full-color LCD display and is the first AED to use...

October 20, 2009 – St. Jude Medical Inc. today said it received European CE mark approval for the industry’s first quadripolar pacing system for cardiac resynchronization therapy defibrillators (...

October 16, 2009 – BIOTRONIK yesterday said it recently received the Industry’s first European CE Mark approval so BIOTRONIK Home Monitoring can replace in-hospital device follow-up visits.

October 15, 2009 – Biosense Webster Inc. said today the U.S. Food and Drug Administration cleared the CARTO 3 System, an advanced 3D imaging technology for use by electrophysiologists in treating...

October 8, 2009 – Boston Scientific Corp. this week announced its exclusive sponsorship and first enrollments of the MADIT-RIT clinical trial, which will determine the best device programming...

October 6, 2009 – New research shows magnetic interference from portable headphones has a clinically significant impact on the function of life-saving devices, according to a new study published...

October 5, 2009 – A reduction in stroke was observed in patients with atrial fibrillation (AF) who received dronedarone (MULTAQ), according to a recent study published online in Circulation – “...

October 2, 2009 – CardioComm Solutions Inc. said yesterday it added the company’s wireless ECG management system to its suite of GEMS (Global ECG Management System) products. GEMS Air builds on...

September 30, 2009 – PLC Systems Inc. demonstrated its RenalGuard System to help prevent contrast-induced nephropathy (CIN) and presented data from its MYTHOS Clinical Trial at the Transcatheter...

September 28, 2009 – Sanofi-aventis announced last week the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMEA) has adopted a positive opinion...

September 28, 2009 - GE Healthcare and Biosense Webster Inc. announced new versions of the Vivid i and Vivid q cardiovascular ultrasound systems, with support for two new intracardiac echo (ICE)...

September 22, 2009 - At the Transcatheter Cardiovascular Therapeutics (TCT) annual meeting Royal Philips Electronics today announced that it will integrate the MAQUET ‘Magnus’ surgical table with...

September 18, 2009 – Physicians at The Mount Sinai Medical Center in New York became the first in the U.S. to ablate atrial fibrillation (AF) using a visually-guided laser balloon catheter.

September 16, 2009 – Texas Cardiac Arrhythmia Institute at St. David’s Medical Center in Austin, Texas plans to create a worldwide electrophysiology (EP) telecardiology network for live...

September 16, 2009 – MemorialCare Heart and Vascular Institute at Long Beach Memorial Medical Center (LBMMC) in Long Beach, Calif., said it implanted a new, heart attack detection device in two...

September 16, 2009 – Hansen Medical Inc. today said it received FDA clearance for its next generation Sensei X Robotic Catheter System and it introduced the Artisan Extend Control Catheter.

...

September 15, 2009 – Fluid monitoring with OptiVol Fluid Status Monitoring is a more accurate predictor of worsening heart failure compared to daily weight monitoring in heart failure patients...

September 15, 2009 – St. Jude Medical Inc. said yesterday the U.S. Food and Drug Administration (FDA) cleared and U.S. launch of the EnSite Velocity Cardiac Mapping System, which is designed to...

September 14, 2009 – The 13th Annual Scientific Meeting of the Heart Failure Society of America (HFSA) today featured four late breaking clinical trials at the Hynes Convention Center in Boston....

September 8, 2009 – Siemens Healthcare and SurgiVision Inc. today announced an agreement for the codevelopment and commercialization of a real-time magnetic resonance image (MRI)-guided cardiac...

September 3, 2009 – ZOLL Medical Corp. received approval from the FDA to market and sell a new model of the LifeVest wearable defibrillator.

September 3, 2009 – Boston Scientific Corp. said Tuesday long-term data from the Prevention of Sudden Cardiac Death II registry (PreSCD II) found that implantable cardioverter defibrillators (ICDs...

September 1, 2009 – St. Jude Medical Inc. today announced European launch of the next generation version 4.0 of its Merlin.net Patient Care Network (PCN), a secure, Internet-based remote care...

August 18, 2009 – Cardiva Medical Inc. recently received FDA clearance for its Cardiva Catalyst III, which the company says is the first drug-coated vascular closure device for the intervention...

August 17, 2009 – Siemens Healthcare will showcase cath lab imaging and workflow enhancements with its hybrid Artis zeego system during the 2009 Transcatheter Cardiovascular Therapeutics Annual...

August 14, 2009 – ZOLL Medical Corp. said today Basingstoke and North Hampshire Hospital in Hampshire, United Kingdom, is the first hospital to install the AutoPulse Noninvasive Cardiac Support...

August 11, 2009 – New research reveals T-wave morphology parameters contain predictive value for mortality in the general population, independent of other clinical risk factors, according to a...

August 5, 2009 – Stereotaxis Inc. said today clinicians performed more than 2,500 procedures with the magnetic irrigated catheter since its commercial release, and the major adverse cardiac event...

August 3, 2009 – Circulatory assist pump maker Thoratec Corp. and small implantable blood pump maker HeartWare International Inc. terminated their merger agreement in response to U.S. Federal...

July 29, 2009 – Transoma Medical Inc., manufacturer of Sleuth AT wireless implantable cardiac monitoring system, today announced the first patient enrollment and implant in a long-term study to...

Jul y 21, 2009 – St. Jude Medical Inc. today said the FDA cleared its Accent RF pacemaker and Anthem RF CRT-P (cardiac resynchronization therapy pacemaker). The company also announced FDA and...

July 20, 2009 - ATS Medical Inc. today announced the first commercial use of the new ATS CryoMaze 10-S Surgical Cryoablation Probe for the treatment of cardiac arrhythmias.

July 17, 2009 – Medtronic announced today the completion of a 12-month follow-up in the STOP-AF (Sustained Treatment of Paroxysmal Atrial Fibrillation) clinical trial evaluating the first...

July 17, 2009 – Medtronic announced today the first enrollments in a magnetic resonance imaging (MRI) substudy of the global PANORAMA registry.

Dr. Raed Sweidan, consultant...

July 13, 2009 – Boston Scientific today announced CE mark for its LATITUDE Patient Management system, used to remotely monitor patients with implantable cardiac devices.

July 9, 2009 – Sorin Group said this week Health Canada cleared the REPLY family of dual- and single-chamber rate adaptive pacemakers.

July 8, 2009 – CardioFocus Inc. said yesterday it received a CE mark in Europe for its Endoscopic Ablation System (EAS) to treat patients with atrial fibrillation.

July 8, 2009 – A procedure that sends targeted energy into the heart through a catheter can be used to treat a common type of irregular heartbeat, but little is known about the treatment's long-...

July 6, 2009 – Sanofi-aventis said last week the FDA approved its Multaq (dronedarone) 400 mg tablets for use in patients with atrial fibrillation (AF) or atrial flutter (AFL).

June 30, 2009 – Physio-Control said yesterday its LUCAS 2 Chest Compression System was granted 510(k) market clearance by the FDA.

Developed and manufactured by Jolife AB and distributed...

June 29, 2009 – Cordex Pharma said today it successfully completed the production of the ATPace clinical trial material (CTM) in preparation for planned pivotal clinical trials. ATPace is a novel...