ClearanceBrief
510(k) K782087 ยท DTB Permanent Pacemaker Electrode

LEAD, SUTURELESS MYOCARDIAL

ApplicantDaig Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 15, 1979
ReceivedDec 14, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782087

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.