ClearanceBrief
510(k) K812905 ยท DTB Permanent Pacemaker Electrode

PERMANENT ENDOCARD. UNIPOLAR TINED LEAD

ApplicantDiag Corp., Walker MI, US
DecisionSubstantially Equivalent, Feb 4, 1982
ReceivedOct 19, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812905

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.