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Cardiac Science Corporation

40 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
9131-001 Defibrillation Electrodes, Lot No. 141125-02 Used in Powerheart G3 9300A, 9300E, recall (Z-0829-2016)Cardiac Science Corporation2016-03-09
Powerheart G3 Automated External Defibrillators (Non-Wearable) and include the following m recall (Z-1057-2012)Cardiac Science Corporation2012-02-27
Powerheart Automated External Defibrillator (AED), G3 is indicated for emergency treatment recall (Z-3265-2011)Cardiac Science Corporation2011-09-19
Automated External Defibrillator (non-wearable). Model number 9200, 9200N, 9200DN, 9200RD, recall (Z-2917-2011)Cardiac Science Corporation2011-08-03
GE Responder 2000 Defibrillator/Monitor, models 2025653, 2026109, and 2026114 that were ma recall (Z-0589-2011)Cardiac Science Corporation2010-12-10
Cardiac Science Powerheart 9390A automated external defibrillator. This fully automatic mo recall (Z-1810-2010)Cardiac Science Corporation2010-06-21
Treadmill models TM55, TM65, and CR60 (brand names include Quinton, Burdick, and Cardiac S recall (Z-1757-2010)Cardiac Science Corporation2010-06-04
Responder 2000 Defibrillator/Monitor Models: 2025653, 2026109, and 2026114. Intended use: recall (Z-1683-2010)Cardiac Science Corporation2010-05-26
Cardiac Science, Automated External Defibrillator (AED) under the following brand names (w recall (Z-1424-2010)Cardiac Science Corporation2010-04-27
Powerheart 9300A automated external defibrillator. This fully automatic model does not req recall (Z-1243-2010)Cardiac Science Corporation2010-04-06
Powerheart 9300E automated external defibrillator. This semi-automatic model requires the recall (Z-1244-2010)Cardiac Science Corporation2010-04-06
Powerheart 9300P automated external defibrillator. This semi-automatic model requires the recall (Z-1245-2010)Cardiac Science Corporation2010-04-06
Powerheart 9390A automated external defibrillator. This fully automatic model does not req recall (Z-1246-2010)Cardiac Science Corporation2010-04-06
Powerheart 9390E automated external defibrillator. This semi-automatic model requires the recall (Z-1247-2010)Cardiac Science Corporation2010-04-06
Responder 2023440 automated external defibrillator. This semi-automatic model requires the recall (Z-1248-2010)Cardiac Science Corporation2010-04-06
Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the recall (Z-1249-2010)Cardiac Science Corporation2010-04-06
Cardiac Science Powerheart 9300A automated external defibrillator. This fully automatic mo recall (Z-0765-2010)Cardiac Science Corporation2010-03-04
Cardiac Science Powerheart 9300C automated external defibrillator. This semi-automatic mod recall (Z-0766-2010)Cardiac Science Corporation2010-03-04
Cardiac Science Powerheart 9300D automated external defibrillator. This semi-automatic mod recall (Z-0767-2010)Cardiac Science Corporation2010-03-04
Cardiac Science Powerheart 9300E automated external defibrillator. This semi-automatic mod recall (Z-0768-2010)Cardiac Science Corporation2010-03-04
Cardiac Science Powerheart 9300P automated external defibrillator. This semi-automatic mod recall (Z-0769-2010)Cardiac Science Corporation2010-03-04
Cardiac Science Powerheart 9390A automated external defibrillator. This fully automatic mo recall (Z-0770-2010)Cardiac Science Corporation2010-03-04
Cardiac Science Powerheart 9390E automated external defibrillator. This semi-automatic mod recall (Z-0771-2010)Cardiac Science Corporation2010-03-04
Burdick Cardiovive 92531 automated external defibrillator. This semi-automatic model requi recall (Z-0772-2010)Cardiac Science Corporation2010-03-04
Burdick Cardiovive 92532 automated external defibrillator. This semi-automatic model requi recall (Z-0773-2010)Cardiac Science Corporation2010-03-04
Burdick Cardiovive 92533 automated external defibrillator. This semi-automatic model requi recall (Z-0774-2010)Cardiac Science Corporation2010-03-04
GE Responder 2019198 automated external defibrillator. This semi-automatic model requires recall (Z-0775-2010)Cardiac Science Corporation2010-03-04
GE Responder 2023440 automated external defibrillator. This semi-automatic model requires recall (Z-0776-2010)Cardiac Science Corporation2010-03-04
NK 9231 CardioLife automated external defibrillator. This semi-automatic model requires th recall (Z-0777-2010)Cardiac Science Corporation2010-03-04
NK 9200G. CardioLife automated external defibrillator. This semi-automatic model requires recall (Z-0778-2010)Cardiac Science Corporation2010-03-04
Cardiac Science Powerheart Automated External Defibrillator G3 9300A recall (Z-0916-2009)Cardiac Science Corporation2009-02-25
Cardiac Science First Save Automated External Defibrillator G3 9300C recall (Z-0917-2009)Cardiac Science Corporation2009-02-25
Cardiac Science Powerheart Automated External Defibrillator G3 9300E. recall (Z-0918-2009)Cardiac Science Corporation2009-02-25
Cardiac Science Powerheart Automated External Defibrillator G3 9390A recall (Z-0919-2009)Cardiac Science Corporation2009-02-25
Cardiac Science Powerheart Automated External Defibrillator G3 9390E recall (Z-0920-2009)Cardiac Science Corporation2009-02-25
Cardio Vive 92532 AED, BURDICK Manufactured by Cardiac Science Corporation, Automated Exte recall (Z-0921-2009)Cardiac Science Corporation2009-02-25
GE Responder 2019198 AED Manufactured for GE Medical Systems Information Technologies by C recall (Z-0922-2009)Cardiac Science Corporation2009-02-25
Electrode Adaptor Cable Quick-Combo System, Model 9055 The 9055 Electrode Adaptor is inten recall (Z-1714-2008)Cardiac Science Corporation2008-09-17
9051 Electrode Adapter; Automated external defibrillator, Used with QUIK-COMBO System; Car recall (Z-1616-2008)Cardiac Science Corporation2008-05-21
Powerheart AED G3 Automated External Defibrillator Model 9300A (Automatic). Cardiac Scienc recall (Z-0623-06)Cardiac Science Corporation2006-03-02

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