ClearanceBrief
510(k) K812832 ยท DXY Implantable Pacemaker Pulse-Generator

MODEL 325C UNIPOLAR CARDIAC PULSE GEN.

ApplicantCook Pacemaker Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 5, 1981
ReceivedOct 9, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812832

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.