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May 29, 2007 — Doctors at University of Pittsburgh Medical School, (UPMC) have begun a study using an investigational ...

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May 29, 2007 — Abbott announced Friday, May 25, that it has initiated a voluntary, nationwide recall of its ARCHITECT ...

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May 29, 2007 — Boston Scientific Corp. has received CE Mark for its TAXUS Liberte Long paclitaxel-eluting coronary stent ...

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May 29, 2007 — The FDA has cleared the Mynx VCS vascular closure system (VCD) by AccessClosure designed to seal a ...

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May 29, 2007 — Orqis Medical Corp., a clinical-stage company developing devices for the treatment of congestive heart ...

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May 29, 2007 — Agfa HealthCare, a leading provider of IT enabled clinical workflow and diagnostic imaging solutions, has ...

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May 29, 2007 — Medtronic Inc. has enrolled the first patient in the landmark PROTECT clinical study, the largest ...

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May 29, 2007 — The FDA has cleared the CORDIS ENTERPRISE Vascular Reconstruction Device and Delivery System under the Humanitarian Device Exemption — it is used with embolic coils for the treatment of intracranial aneurysms. It consists of a self-expanding stent and a delivery system. The stent serves as a scaffold for embolic coils to prevent herniation of the coils into the parent vessel.

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May 29, 2007 — Abbott announced positive results last week from ABSORB, the world’s first clinical trial evaluating the ...

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May 23, 2007 — InspireMD has announced this week the enrollment of 19 patients in its First in Man study in a ...

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May 22, 2007 — Luna Innovations has announced it has received a market clearance letter in response to its 510(k) ...

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May 23, 2007 — MicroMed Cardiovascular Inc. has announced that on Monday, May 14, 2007, doctors at Freeman Hospital in ...

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May 23, 2007 — MedicalCV Inc. has announced that the United States Patent and Trademark Office ("USPTO") has issued ...

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May 23, 2007 — XTENT Inc. announced positive six-month follow-up data from the CUSTOM II clinical trial, which assessed ...

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May 21, 2007 — Sanofi-aventis has announced that the FDA has approved a supplemental New Drug Application (sNDA) for the ...

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