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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K040438
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Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs ar... 2 01/15/2005 FEI # 2112020
Cardiac Science, Inc.
Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Science AEDs ar... 2 03/02/2006 FEI # 2112020
Cardiac Science Corporation
Cardio Vive 92532 AED, BURDICK Manufactured by Cardiac Science Corporation, Automated External Defi... 2 02/25/2009 FEI # 2112020
Cardiac Science Corporation
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