ClearanceBrief
510(k) K910528 ยท DTB Permanent Pacemaker Electrode

BIPOLAR SUTURELESS MYOCARDIAL PACING LEADS

ApplicantPossis Medical, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Aug 9, 1991
ReceivedFeb 8, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910528

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.