ClearanceBrief
510(k) K780446 ยท DTB Permanent Pacemaker Electrode

SUTURELESS MYOCARDIAL PACING LEAD

ApplicantMedtronic Vascular MD, US
DecisionSubstantially Equivalent, May 19, 1978
ReceivedMar 20, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780446

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.