ClearanceBrief
510(k) K042088 ยท MKJ Automated External Defibrillators (Non-Wearable)

SAMARITAN PAD PAK DEFIBRILLATION ELECTRODE, MODEL SPP-301

ApplicantHeartsine Technologies, Inc., San Clemente CA, US
DecisionSubstantially Equivalent, Sep 2, 2004
ReceivedAug 3, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K042088

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.