ClearanceBrief
510(k) K912867 ยท DTB Permanent Pacemaker Electrode

OSCOR MEDICAL CORP PERMANENT PACING LEAD

ApplicantOscor Medical Corp., Palm Harbor FL, US
DecisionSubstantially Equivalent, Feb 4, 1992
ReceivedJun 28, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912867

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.