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April 9, 2007 — The drug used in Johnson & Johnson’s drug-eluting stent — produced by J&J-owned Cordis — does not ...

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April 9, 2007 — MIV Therapeutics Inc. has announced that its recent bench test confirmed that merging Biosync Scientific ...

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April 6, 2007 — Toshiba America Medical Systems, Inc. has developed three imaging techniques for its MR product line ...

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April 6, 2007 — Spectranetics Corp., Colorado Springs, CO, has announced the commercial availability of the TURBO elite ...

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April 6, 2007 — Ohio State University Heart Center has appointed cardiac ultrasound expert Dr. Thomas Ryan as its new director. Dr. Ryan was director of the Duke University Heart Center.

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April 6, 2007 — MedicalCV Inc., Minneapolis, MN, has announced that Allen R. Raczkowski, M.D., director of Robotic Cardiac Surgery at Banner Baywood Health Systems in Mesa, AZ, performed a closed-chest, robotic, lone cardiac ablation procedure on an arrested heart on March 30 using the ATRILAZE Surgical Ablation System.

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Technology

The AXIOM Sensis XP combines both hemo and advanced EP applications in one system. The system delivers clinical workflow ...

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The AXIOM Sensis XP combines both hemo and advanced EP applications in one system. The system delivers clinical workflow ...

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April 4, 2007 — Vital Images, Inc., a leading provider of enterprise-wide advanced visualization and analysis software ...

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April 4, 2007 — Immersion Medical has updated its endovascular platform with features that allow it to simulate a wider ...

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April 4, 2007 — A Japanese study has shown that people who take statins and also consume omega-3 fatty acids, typically ...

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April 4, 2007 — Stereotaxis, Inc. has announced that its partnered magnetically enabled 8mm ablation catheter has received FDA approval and will soon be commercially available in the U.S. Two leading European electrophysiology centers have been building successful clinical experience using this catheter to treat atrial cardiac arrhythmias.

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April 4, 2007 — Volcano Corp. and ev3 Inc. have announced they have entered into a joint marketing and distribution ...

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Cardica Inc. has announced that it has received FDA 510(k) clearance to market its C-Port Flex A Anastomosis System in ...

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April 3, 2007 —FoxHollow Technologies Inc. has announced it has submitted a 510(k) premarket notification to the U.S. Food and Drug Administration for its NightHawk Plaque Excision System. The intended use of the NightHawk System is in the evaluation of peripheral vascular morphology.

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