ClearanceBrief
510(k) K771626 ยท DXY Implantable Pacemaker Pulse-Generator

PACEMAKER MODEL 251

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 12, 1977
ReceivedAug 25, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K771626

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.