ClearanceBrief
510(k) K822904 ยท DXY Implantable Pacemaker Pulse-Generator

MODEL 325D UNIPOLAR CARDIAC PULSE GEN

ApplicantCook Pacemaker Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 15, 1982
ReceivedSep 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822904

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.