ClearanceBrief
510(k) K780246 ยท DTB Permanent Pacemaker Electrode

PACEMAKER, ELECTRODE, PERMANENT & TEMP.

ApplicantDaig Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 31, 1978
ReceivedFeb 13, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780246

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.