ClearanceBrief
510(k) K790074 ยท DTB Permanent Pacemaker Electrode

MEDTRONIC MODEL 6971

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Mar 29, 1979
ReceivedJan 11, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K790074

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.