ClearanceBrief
510(k) K770880 ยท DXY Implantable Pacemaker Pulse-Generator

GENERATOR, PULSE, UNIPOLAR, #508

ApplicantCardiac Pacemakers, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 20, 1977
ReceivedMay 16, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770880

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.