The FDA has cleared St. Jude Medical’s Reflexion Spiral Variable Radius Mapping Catheter featuring a circular loop at ...
Like medieval knights in battle, stent-wielding cath-lab doctors arm themselves with heavy and cumbersome lead garments ...
The first automated tiered storage appliance integrates ABREVITY’s FileData Classifier software, QStar’s Hierarchical ...
Cardiac PET/CT represents a major advancement in cardiovascular diagnostics, offering significant clinical and ...
Boston Scientific’s LATITUDE 2.0 software with LATITUDE remote data integration capabilities is now FDA cleared ...
Feb. 7, 2007 — Abbott has announced its plan to launch the world's first drug-eluting stent clinical trial solely in ...
Feb. 6, 2007 — The Centers for Medicare and Medicaid Services (CMS) has released new proposed policy in which coverage ...
SPONSORED CONTENT — Studycast is a comprehensive imaging workflow system that allows healthcare professionals to work ...
Feb. 6, 2007 — The FDA has issued an approval letter for GlaxoSmithKline’s once-a-day anticoagulant, Arixtra ...
Feb. 1, 2007 — Royal Philips Electronics has announced the commercial release of its new EP Navigator, which Philips ...
Feb. 1, 2007 — Cook Medical released nine-month data this week for its PTX Paclitaxel-Eluting Stent (DES) trial, which ...
Providing exceptional cardiovascular care for patients to achieve the best possible outcomes is the number one goal for ...
Feb. 1, 2007 - New data shows that a year after undergoing carotid angioplasty and stenting, a minimally invasive ...
Feb. 1, 2007 — Stockholders of Conor Medsystems, Inc. have approved the merger agreement between Conor and Johnson & ...
Jan. 31, 2007 — Researchers said this week that they have found an implantable wireless sensor that monitors blood pressure in an aneurysm sac to be safe and useful in guiding endovascular repair of an abdominal aortic aneurysm (AAA).
Cardiac positron emission tomography (PET) is growing in popularity among cardiologists because it provides the ability ...
Jan. 31, 2007 — Boston Scientific Corp. days it has received FDA 510(k) clearance to expand its PolarCath Peripheral Dilatation System offering to include a 100mm balloon.
Jan. 31, 2007 — Possis Medical, Inc., a developer, manufacturer and distributor of endovascular medical devices, announced yesterday that it has FDA approval to being marketing AngioJet Spiroflex rapid exchange catheter to remove blood clots (thrombus) from coronary arteries.
Jan. 31, 2007 — Physicians at Brigham and Women’s Hospital and Harvard Medical School have published study results in ...
February 06, 2007
