ClearanceBrief
510(k) K031274 ยท DTB Permanent Pacemaker Electrode

MODEL 5071 MYOCARDIAL PACING LEAD

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., May 22, 2003
ReceivedApr 22, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031274

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.