Technology

The completely redesigned EXCELART Vantage Atlas 1.5T MRI system from Toshiba features 128 elements that deliver high ...

Home February 06, 2007
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Technology

The FDA has cleared St. Jude Medical’s Reflexion Spiral Variable Radius Mapping Catheter featuring a circular loop at ...

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Feature | Mark Paquin

Author’s Note: For this inaugural article I begin with an insider’s look on the “health” of drug-eluting stents and what lies ahead for this much-debated device.

Home February 06, 2007
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Technology

The first automated tiered storage appliance integrates ABREVITY’s FileData Classifier software, QStar’s Hierarchical ...

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Boston Scientific’s LATITUDE 2.0 software with LATITUDE remote data integration capabilities is now FDA cleared ...

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Feb. 7, 2007 — Abbott has announced its plan to launch the world's first drug-eluting stent clinical trial solely in ...

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Feature | Kim Phelan

Status quo is probably not a phrase in Dr. Cynthia Tracy’s professional vocabulary, because, in her daily combat against ...

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Feb. 6, 2007 — The Centers for Medicare and Medicaid Services (CMS) has released new proposed policy in which coverage ...

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Feb. 6, 2007 — The FDA has issued an approval letter for GlaxoSmithKline’s once-a-day anticoagulant, Arixtra ...

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Feb. 1, 2007 — Royal Philips Electronics has announced the commercial release of its new EP Navigator, which Philips ...

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Feb. 1, 2007 — Cook Medical released nine-month data this week for its PTX Paclitaxel-Eluting Stent (DES) trial, which ...

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Feb. 1, 2007 - New data shows that a year after undergoing carotid angioplasty and stenting, a minimally invasive ...

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Feb. 1, 2007 — Stockholders of Conor Medsystems, Inc. have approved the merger agreement between Conor and Johnson & ...

Home January 31, 2007
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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).

Home January 30, 2007
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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.

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