ClearanceBrief
510(k) K772203 ยท DTB Permanent Pacemaker Electrode

VENTRICULAR LEADS

ApplicantMedtronic Vascular, Walker MI, US
DecisionSubstantially Equivalent, Jan 11, 1978
ReceivedNov 30, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K772203

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.