ClearanceBrief
510(k) K772103 ยท DTB Permanent Pacemaker Electrode

BIPOLAR LEADS, DISP.

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Nov 21, 1977
ReceivedNov 7, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772103

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.