ClearanceBrief
510(k) K911048 ยท DTD Pacemaker Lead Adaptor

MODEL 5857-3M LEAD END CAP KIT

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Apr 18, 1991
ReceivedMar 8, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911048

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.