ClearanceBrief
510(k) K844857 ยท DTD Pacemaker Lead Adaptor

PACESETTER SYSTEMS, INC. ENDOCARDIAL SCREW-IN LEAD

ApplicantPacesetter Systems, Sylmar CA, US
DecisionSubstantially Equivalent, Feb 14, 1985
ReceivedDec 14, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844857

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.