ClearanceBrief
510(k) K802864 ยท DXY Implantable Pacemaker Pulse-Generator

SIEMENS-ELEMA PULSE GENERATOR 678

ApplicantSiemens Elema AB, Mchenry IL, US
DecisionSubstantially Equivalent, Feb 5, 1981
ReceivedNov 12, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802864

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.