ClearanceBrief
510(k) K781864 ยท DTD Pacemaker Lead Adaptor

ADAPTER KIT

ApplicantDaig Corp., Walker MI, US
DecisionSubstantially Equivalent, Dec 19, 1978
ReceivedNov 6, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781864

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.