ClearanceBrief
510(k) K142709 ยท MKJ Automated External Defibrillators (Non-Wearable)

samaritan PAD 450P

ApplicantHeartsine Technologies, Inc., Newton PA, US
DecisionSubstantially Equivalent, Mar 27, 2015
ReceivedSep 22, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K142709

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.