ClearanceBrief
510(k) K801039 ยท DTD Pacemaker Lead Adaptor

ADAPTAID HELICAL COIL ADAPTER 365-14

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 21, 1980
ReceivedMay 2, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801039

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.