ClearanceBrief
510(k) K022929 ยท MKJ Automated External Defibrillators (Non-Wearable)

PEDIATRIC ATTENUATED DEFIBRILLATION ELECTRODES, MODEL 9730, POWEDERHEART AED, MODEL 9200/9210

ApplicantCardiac Science, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Jan 27, 2003
ReceivedSep 4, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K022929

No recall in the FDA data names this 510(k).

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