ClearanceBrief
510(k) K820935 ยท DTD Pacemaker Lead Adaptor

MODEL 5866-26 LEAD ADAPTER KIT

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Apr 16, 1982
ReceivedApr 2, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820935

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.