ClearanceBrief
510(k) K780623 ยท DTB Permanent Pacemaker Electrode

ENDOCARDIAL ATRIAL PACING LEAD, M. 6994

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Jul 28, 1978
ReceivedApr 14, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780623

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.