ClearanceBrief
510(k) K812517 ยท LDF Electrode, Pacemaker, Temporary

CARDIAC PACING ELECTRODES

ApplicantMedics Instrument Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 13, 1981
ReceivedSep 2, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812517

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.