ClearanceBrief
510(k) K033144 ยท MKJ Automated External Defibrillators (Non-Wearable)

DEFIBTECH ELECTRODE ADAPTER, MODEL DAC-300 SERIES

ApplicantDefibtech, LLC, Guilford CT, US
DecisionSubstantially Equivalent, Nov 13, 2003
ReceivedSep 30, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033144

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.