ClearanceBrief
510(k) K801038 ยท DTD Pacemaker Lead Adaptor

ADAPTAID ELEMA LEAD ADAPTER KIT 365-17

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 8, 1980
ReceivedMay 2, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801038

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.