Home » FDA APPROVES GUIDANT'S NEW DEFIBRILLATOR
FDA APPROVES GUIDANT'S NEW DEFIBRILLATOR
The FDA recently approved a new implantable cardioverter defibrillator (ICD), developed by Guidant.
The Vitality HE device is capable of delivering more energy than Guidant's previous ICDs, the company said. These devices are used to shock a dangerously irregular heartbeat back to normal. Guidant will launch the new ICD this month.
KEYWORDS FDAnews Device Daily Bulletin
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