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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 33 Results
510(K) Number: K031987
 
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Power Heart AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9142 2 07/20/2004 FEI # 2112020
Cardiac Science, Inc.
FirstSave AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9143 2 07/20/2004 FEI # 2112020
Cardiac Science, Inc.
Powerheart AED G3 Automated External Defibrillator Model 9300E. Cardiac Science AEDs are manufactur... 2 01/15/2005 FEI # 2112020
Cardiac Science, Inc.
Cardiac Science Powerheart Automated External Defibrillator G3 9300A 2 02/25/2009 FEI # 2112020
Cardiac Science Corporation
Cardiac Science First Save Automated External Defibrillator G3 9300C 2 02/25/2009 FEI # 2112020
Cardiac Science Corporation
Cardiac Science Powerheart Automated External Defibrillator G3 9300E. 2 02/25/2009 FEI # 2112020
Cardiac Science Corporation
Cardiac Science Powerheart Automated External Defibrillator G3 9390A 2 02/25/2009 FEI # 2112020
Cardiac Science Corporation
Cardiac Science Powerheart Automated External Defibrillator G3 9390E 2 02/25/2009 FEI # 2112020
Cardiac Science Corporation
Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requires the u... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
NK 9200G. CardioLife automated external defibrillator. This semi-automatic model requires the user ... 1 03/04/2010 FEI # 2112020
Cardiac Science Corporation
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