ClearanceBrief
510(k) K800354 ยท DTB Permanent Pacemaker Electrode

LEAD, TINED PACING, IMPLANTABLE

ApplicantDaig Corp., Mchenry IL, US
DecisionSubstantially Equivalent, May 30, 1980
ReceivedFeb 15, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800354

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.