ClearanceBrief
510(k) K851699 ยท DXY Implantable Pacemaker Pulse-Generator

COOK PACEMAKER CORP. 332T BIPOLAR CARDIAC PULSE GE

ApplicantCook Pacemaker Corp., Leechburg PA, US
DecisionSubstantially Equivalent, May 16, 1985
ReceivedApr 24, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851699

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.