The U.S. Food and Drug Administration (FDA) has cleared Sotera Wireless Inc.’s patented continuous non-invasive blood pressure (cNIBP) technology, a new feature of the ViSi Mobile wireless patient monitoring system. For the first time clinicians can continuously monitor all patient vital signs, including beat-to-beat blood pressure, without the use of a catheter or blood pressure cuff.
The Boston Scientific OffRoad Re-Entry Catheter System demonstrated excellent performance in facilitating the treatment of complete blockages in the major arteries that supply blood to the legs. These blockages, called chronic total occlusions (CTOs), are often associated with peripheral artery disease (PAD). The data from the Re-ROUTE clinical trial were reported in a late-breaking clinical trial session at the Vascular Interventional Advances Conference (VIVA) in Las Vegas.
AccessClosure Inc. announced an exclusive agreement with Ostial Corp. to distribute the Flash Ostial System Dual Balloon Angioplasty Catheter in the United States. The system is designed to help overcome the challenges of aorto-ostial stenting and complements the Mynx product family of vascular closure devices.
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CardioDx Inc. announced results of two studies indicating that Corus CAD, a blood-based gene expression test, may help reduce unnecessary cardiac testing and costs by aiding clinician decision-making in the evaluation of women with obstructive coronary artery disease (CAD) symptoms. The studies were presented at The North American Menopause Society (NAMS) 2013 Annual Meeting in Dallas, Texas.

High levels of high-density lipoprotein (HDL) have been linked to increased breast cancer risks and enhanced cancer aggressiveness in animal experiments.
Preventice Inc. has received CE mark certification for its BodyGuardian remote monitoring system.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
Bioventrix announced the presentation of scientific data demonstrating the durability of its Revivent Myocardial Anchoring System in 24 patients one year post-procedure. The data, which Andrew Wechsler, M.D. and professor of cardiothoracic surgery, Drexel University, presented at the prestigious European Association for Cardio-Thoracic Surgery meeting in Vienna, Austria, highlighted results from the company’s Phase I clinical trial conducted at five European centers.

A mother and her 25-week-old fetus are doing well after a team of physicians performed a successful in utero cardiac interventional procedure on the fetus at California Hospital Assn. (CHA) Hollywood Presbyterian Medical Center.
Mortara Instrument Inc. announced an integrated connectivity solution that provides data from the Quinton Q-Tel Rehabilitation Management Systems to the American Association of Cardiovascular and Pulmonary Rehabilitation’s (AACVPR’s) Outpatient Cardiac Rehabilitation Registry. The web-based registry is the first of its kind in the United States and will provide cardiac rehabilitation professionals with a means to track, document and communicate patient outcomes and program performance.
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
Critical Diagnostics announced that results of the Heart Failure: A Controlled Trial Investigating Outcomes of Exercise (HF-Action) study published in the American Heart Association’s (AHA’s) Circulation: Heart Failure demonstrates that levels of the biomarker ST2 are predictive of long-term outcomes for people suffering with heart failure and identify those patients who may benefit from exercise.
Biotronik announced the launch of the new Idova 7 series. Idova 7 ICDs (implantable cardioverter-defibrillators) and CRT-Ds (cardiac resynchronization therapy defibrillators)offer ultrahigh-energy therapy without compromising on short charge times (10 seconds), smaller size (34 cc) and longevity of more than 11 years. Designed to stop life-threatening arrhythmias with the very first shock, Idova 7 gives patients valuable peace of mind.
MAM-A Inc., a recordable discs supplier, announced its partnership with TEAC Corp. for the sales of the UR-50BD High Definition (HD) Medical Image Recorder. The medical image recorder is available together with medical-grade recordable DVDs, Blu-ray discs, or USB flash drives and is ideal for radiology, angiography, fluoroscopy, endoscopy and ultrasound. Discs and flash drives can have hospital logos imprinted on the surfaces if requested.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
IMRIS Inc. and Siemens Healthcare announced an agreement that positions one of Siemens’s computed tomography (CT) products as the core of the IMRIS Visius iCT solution.
At RSNA 2013, ContextVision will announce its latest additions to its U.S. PlusView Family, which will include four different packages for women’s health, general imaging, cardiovascular and point of care (POC). More anatomically correct images provide medical professionals diagnostic confidence for the most complex patient cases.
The U.S. Food and Drug Administration's (FDA) Circulatory Systems Devices Advisory Panel this week voted that biventricular (BiV) pacing with Medtronic Inc. devices is beneficial for treating patients who have atrioventricular (AV) block and left ventricular (LV) systolic dysfunction, compared to conventional right ventricular pacing.