ClearanceBrief
510(k) K832255 ยท DTB Permanent Pacemaker Electrode

MODEL F UNIPOLAR ENDOCARDIAL LEAD-

ApplicantCook Pacemaker Corp., Walker MI, US
DecisionSubstantially Equivalent, Aug 12, 1983
ReceivedJul 11, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832255

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.