ClearanceBrief
510(k) K841230 ยท DXY Implantable Pacemaker Pulse-Generator

PULSE GENERATOR 686, 686B 686L

ApplicantSiemens Elema AB, Mchenry IL, US
DecisionSubstantially Equivalent, Dec 3, 1984
ReceivedMar 22, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841230

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.