ClearanceBrief
510(k) K792379 ยท DTB Permanent Pacemaker Electrode

CARDIAC PACING ELECTRODE

ApplicantMedi-Dyne Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 5, 1979
ReceivedNov 26, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792379

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.