ClearanceBrief
510(k) K873728 ยท LDF Electrode, Pacemaker, Temporary

DEKNATEL TEMPORARY CARDIAC PACING WIRE

ApplicantDeknatel, Inc., Lake Success NY, US
DecisionSubstantially Equivalent, Nov 3, 1987
ReceivedSep 16, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873728

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.