ClearanceBrief
510(k) K800795 ยท DTB Permanent Pacemaker Electrode

PERMANENT & TEMP. PACEMAKER ELECTRODE

ApplicantDaig Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 30, 1980
ReceivedApr 9, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800795

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.