ClearanceBrief
510(k) K895525 ยท DRL Tester, Defibrillator

MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER

ApplicantMatrix Medica, Inc., Orchard Park NY, US
DecisionSubstantially Equivalent, Jan 26, 1990
ReceivedSep 12, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895525

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.