ClearanceBrief
510(k) K832052 ยท DXY Implantable Pacemaker Pulse-Generator

MODEL 327T UNIPOLAR CARDIAC PULSE GEN

ApplicantCook Pacemaker Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 8, 1983
ReceivedJun 27, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832052

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.