ClearanceBrief
510(k) K802552 ยท DTB Permanent Pacemaker Electrode

PERM. ENDOCARDIAL UNIPOLAR TINED/WEDGE

ApplicantDaig Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 16, 1981
ReceivedOct 15, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802552

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.