ClearanceBrief
510(k) K801040 ยท DTD Pacemaker Lead Adaptor

GE LEAD ADAPTER, MODEL 345-01

ApplicantIntermedics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 30, 1980
ReceivedMay 2, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801040

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.