ClearanceBrief
510(k) K813576 ยท DXY Implantable Pacemaker Pulse-Generator

SIEMENS-ELEMA PULSE GENERATOR 659

ApplicantSiemens Elema AB, Mchenry IL, US
DecisionSubstantially Equivalent, Jan 22, 1982
ReceivedDec 23, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813576

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.