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Cardiac Science Corporation: 510(k) Clearances

21 510(k) clearances from Oct 16, 1997 to May 4, 2015, newest first. Showing 1 to 21.

What this list covers: FDA records filed under the name "Cardiac Science Corporation" and its spelling variant "Cardiac Science".

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K-NumberDeviceDate
K143714Powerheart G5 AEDMay 4, 2015
K122758POWERHEART G5 AEDFeb 12, 2014
K113176MYSENSE HEARTDec 21, 2011
K102496POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED…Jun 9, 2011
K093211CARECENTER MDJun 3, 2010
K091943POWERHEART AED G3, MODEL 9390E, POWERHEART AED G3 AUTOMATIC, MODEL 9390ASep 10, 2009
K0820909131 DEFIBRILLATION ELECTRODESDec 12, 2008
K082173Q-STRESS AND HEARTSTRIDE, MODELS QSTRESS/Q40 AND H4/H4SAug 26, 2008
K060934MODIFICATION TO POWERHEART ECDMay 15, 2006
K060167ATRIA 3100, ATRIA 6100Apr 19, 2006
K052316POWERHEART ECDJan 3, 2006
K052161POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A)Oct 21, 2005
K040637POWERHEART AED G3 PROAug 6, 2004
K040438POWERHEART AED G3AJul 1, 2004
K031987POWERHEART AED G3, MODEL 9300Jul 30, 2003
K022929PEDIATRIC ATTENUATED DEFIBRILLATION ELECTRODES, MODEL 9730, POWEDERHEART AED, MODEL 9200/9210Jan 27, 2003
K022210MULTIFUNCTIONAL ELECTRODE MODELS 9640, 9650Oct 4, 2002
K012197POWERHEART CARDIAC RHYTHM MODULENov 16, 2001
K993533POWERHEART AECDJan 24, 2000
K982710AECD ARRHYTHMIA DETECTION SOFTWAREAug 10, 1998
K970741POWERHEART AECDOct 16, 1997

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.