ClearanceBrief
510(k) K091943 ยท MKJ Automated External Defibrillators (Non-Wearable)

POWERHEART AED G3, MODEL 9390E, POWERHEART AED G3 AUTOMATIC, MODEL 9390A

ApplicantCardiac Science Corporation, Bothell WA, US
DecisionSubstantially Equivalent, Sep 10, 2009
ReceivedJun 30, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K091943

DateFirm and productCodeLinked 510(k)
Apr 6, 2010Cardiac Science Corporation
Powerheart 9300A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Brand na
Terminated
MKJNone listed
Apr 6, 2010Cardiac Science Corporation
Powerheart 9300E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Br
Terminated
MKJNone listed
Apr 6, 2010Cardiac Science Corporation
Powerheart 9300P automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Br
Terminated
MKJNone listed
Apr 6, 2010Cardiac Science Corporation
Powerheart 9390A automated external defibrillator. This fully automatic model does not require the user to press a shock button in order for the device to deliver therapy (when appropriate). Brand n
Terminated
MKJNone listed
Apr 6, 2010Cardiac Science Corporation
Powerheart 9390E automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Br
Terminated
MKJNone listed
Apr 6, 2010Cardiac Science Corporation
Responder 2023440 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). B
Terminated
MKJNone listed
Apr 6, 2010Cardiac Science Corporation
Cardiovive 92532 automated external defibrillator. This semi-automatic model requires the user to press a shock button in order for the device to deliver defibrillation energy (when appropriate). Br
Terminated
MKJNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.