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The FDA will convene a Medical Device Dispute Resolution Panel (MDDRP) on Dec. 15 to consider the first device to ...

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The Laboratory Services unit of Rheologics has launched a Whole Blood Viscosity (WBV) testing program for physicians ...

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Cardiac Science has begun shipping its news Powerheart G3 Plus, a CPR-enhanced addition to the Powerheart automated ...

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MicroMed Cardiovascular, Inc. has received a CE Mark extension to continue marketing its DeBakey VAD system in Europe ...

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The FDA panel that convened for an intense, two-day review of drug-eluting stents last week heard key testimony from ...

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A strong grassroots effort among physicians played a key role in staving off a Medicare physician payment cut that would ...

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FUJIFLM Medical Systems USA, Inc. (“Fuji”) and Problem Solving Concepts, Inc. (“ProSolv”) have announced a co-marketing ...

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Agfa HealthCare has signed a contract with the National Heart Centre (NHC) of Singapore, the national referral centre ...

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The FDA panel that is re-evaluating the safety of drug-eluting stents convenes Dec. 7 and 8 at the Hilton Washington DC ...

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Taking anti-platelet medication longer than current recommendations may lower heart attack or death risks for patients ...

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Phase III of CoreValve’s international trial for its patented 18-French Revalving System is now one-third enrolled since ...

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The FDA was notified on Dec. 2 that Pfizer will suspend a large, Phase 3 trial evaluating the investigational ...

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The FDA will revisit a device tomorrow that it cleared for U.S. sale three years ago — drug-eluting stents will be the ...

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The American Heart Association has published a report demonstrating that adolescent boys have a significantly increased ...

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Feature | Judy Harvey

Pulse oximetry, which directly monitors the patient's oxygenation, came into its own as standard medical practice 20 ...

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