ClearanceBrief
510(k) K851890 ยท DTD Pacemaker Lead Adaptor

MEDTRONIC 5064

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Jun 19, 1985
ReceivedApr 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851890

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.