ClearanceBrief
510(k) K772226 ยท DXY Implantable Pacemaker Pulse-Generator

PACEMAKER, MODEL 225 & 227

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 27, 1978
ReceivedDec 6, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772226

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.