ClearanceBrief
510(k) K802816 ยท DTB Permanent Pacemaker Electrode

ENDOCARDIAL LEADS 414S & 515S

ApplicantSiemens Elema AB, Mchenry IL, US
DecisionSubstantially Equivalent, Jan 16, 1981
ReceivedNov 7, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802816

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.