ClearanceBrief
510(k) K791769 ยท DTB Permanent Pacemaker Electrode

MEDTRONIC MODEL 6957

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Sep 19, 1979
ReceivedSep 5, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791769

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.