ClearanceBrief
510(k) K012452 ยท LDF Electrode, Pacemaker, Temporary

MODEL 6500 UNIPOLAR TEMORARY MYOCARDIAL PACING LEAD

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 14, 2001
ReceivedAug 1, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K012452

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.