ClearanceBrief
510(k) K854128 ยท DTB Permanent Pacemaker Electrode

OSCOR MEDICAL UNIPOLAR PERMANENT PACING LEAD-CONNE

ApplicantOscor Medical Corp., Palm Harbor FL, US
DecisionSubstantially Equivalent, Feb 26, 1986
ReceivedOct 9, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854128

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.