ClearanceBrief
510(k) K832099 ยท DTB Permanent Pacemaker Electrode

MEDTRONIC MODELS 4012 & 4512

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Jul 26, 1983
ReceivedJun 29, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832099

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.