ClearanceBrief
510(k) K854919 ยท DXY Implantable Pacemaker Pulse-Generator

BIPOLAR CARDIAC PULSE GENERATOR WITH TELEMETRY

ApplicantCook Pacemaker Corp., Leechburg PA, US
DecisionSubstantially Equivalent, Dec 19, 1985
ReceivedDec 9, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854919

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.