ClearanceBrief
510(k) K854963 ยท DTB Permanent Pacemaker Electrode

S80 IMPLANTABLE CARDIAC PACING LEAD

ApplicantSorin Biomedica, Fiat, USA, Inc., Italy, IT
DecisionSubstantially Equivalent, Jun 24, 1986
ReceivedDec 11, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854963

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.