ClearanceBrief
510(k) K843060 ยท DTD Pacemaker Lead Adaptor

SENTRA

ApplicantCardiac Pacemakers, Inc., Walker MI, US
DecisionSubstantially Equivalent, Sep 20, 1984
ReceivedAug 3, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843060

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.