ClearanceBrief
510(k) K082090 ยท MKJ Automated External Defibrillators (Non-Wearable)

9131 DEFIBRILLATION ELECTRODES

ApplicantCardiac Science Corporation, Bothell WA, US
DecisionSubstantially Equivalent, Dec 12, 2008
ReceivedJul 24, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K082090

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.