October 3, 2012 — Royal Philips Electronics announced it is donating the one-millionth HeartStart automated external defibrillator (AED) manufactured to Everett Mountain Rescue Unit (EMRU) of Snohomish, Wash. EMRU is a volunteer search and rescue organization serving Snohomish County, also the location of Philips’ HeartStart headquarters.
October 3, 2012 — Sharp Memorial Hospital was the first on the West Coast to participate in Medtronic's SYMPLICITY HTN-3 clinical trial in March, and is currently the leading trial site in Southern California, to test an experimental medical device that aims to lower high blood pressure by using radio frequency energy to disrupt hyperactive nerves that contribute to the condition.
October 3, 2012 — Stentys, a medical technology company commercializing the world's first and only self-apposing stent to treat acute myocardial infarction (AMI), announced today the European commercial release of an enhanced stent-delivery system for its Self-Apposing stent.
SPONSORED CONTENT — Studycast is a comprehensive imaging workflow system that allows healthcare professionals to work ...
October 2, 2012 — AstraZeneca has announced the results from a sub-analysis of PLATO that evaluated the effects of age on clinical outcomes in patients with acute coronary syndrome (ACS). Results of the analysis suggest the overall findings from the PLATO study of a greater reduction in thrombotic cardiovascular (CV) events with Brilinta (ticagrelor) tablets plus aspirin compared to clopidogrel plus aspirin were consistent regardless of age.
Terumo Cardiovascular Systems has announced the introduction of the VirtuoSaph Plus Endoscopic Vessel Harvesting System following clearance by the U.S. Food and Drug Administration (FDA).
October 2, 2012 — A new survey of physicians shows that if the U.S. presidential election were held today, 55 percent would vote for Mitt Romney and 36 percent would support President Barack Obama, according to a survey conducted by Jackson & Coker, a division of Jackson Healthcare, the third largest healthcare staffing company in the United States.
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
October 2, 2012 — A novel blood thinner recently approved by the U.S. Food and Drug Administration (FDA), Pradaxa (dabigatran), has been rapidly adopted into clinical practice, yet thus far has had little impact on improving treatment rates for atrial fibrillation.
October 1, 2012 — Effective immediately, Ziehm Imaging, a market leader for mobile C-arms, is offering operating room (OR) tables from the Swedish manufacturer Stille to complement its Ziehm Vision RFD Hybrid Edition.
October 1, 2012 — Bristol-Myers Squibb Company and Pfizer Inc. announced that the U.S. Food and Drug Administration (FDA) has acknowledged receipt of the new drug application (NDA) resubmission for Eliquis (apixaban) to reduce the risk of stroke and systemic embolism in patients with nonvalvular atrial fibrillation (NVAF).
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
October 1, 2012 — SunTech Medical’s One-Piece Durable Cuffs are a new line of easily disinfected, reusable cuffs for reliable blood pressure monitoring. The highly durable cuffs feature a cost-effective, one-piece design sturdy enough for repeated use in any clinical environment.
October 1, 2012 — CircuLite Inc. announced that the latest data from patients enrolled in the company’s CE mark trial of the Synergy Circulatory Support System strengthened prior findings indicating that implantation with Synergy resulted in significant, sustained improvements in hemodynamics and exercise tolerance.
September 28, 2012 — MindChild Medical Inc. announced that it has received 510(k) premarketing notification clearance from the U.S. Food and Drug Administration (FDA) for its Meridian noninvasive fetal heart monitor, and anticipates entering the U.S. market with Meridian soon. Additional pre-market regulatory filings are anticipated during 2012 and 2013.
When performing radiofrequency (RF) ablation to treat cardiac arrhythmia, medical professionals must balance the safety ...
September 28, 2012 — Accumetrics Inc., developer of the VerifyNow System, the first rapid and easy-to-use point-of-care system for measuring platelet reactivity to multiple antiplatelet agents, announced the launch of its Quality Improvement and Value Assessment Program.

The world’s first drug-eluting bioabsorbable vascular scaffold has been launched and will revolutionize the stent industry. On Sept. 25, 2012, Abbott announced the launch of its drug-eluting bioabsorbable stent, Absorb, in Europe, the Middle East and parts of Asia Pacific and Latin America. Absorb, which received CE mark certification in 2011, is used to treat coronary artery disease. Bioabsorbable stents, such as Absorb, will broaden treatment and diagnostic options, reduce the need for long-term anti-platelet therapy and reduce the risk of in-stent restenosis and thrombosis.
September 28, 2012 — Boston Scientific Corp. announced it has received U.S. Food and Drug Administration (FDA) clearance for the Emerge percutaneous transluminal coronary angioplasty (PTCA) balloon dilatation catheter, and has begun marketing the device in the United States.