ClearanceBrief
510(k) K904868 ยท LDF Electrode, Pacemaker, Temporary

XEMEX TEMPORARY PACING CATHETER A

ApplicantZeon Medical Corp., White Plains NY, US
DecisionSubstantially Equivalent, May 16, 1991
ReceivedOct 29, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904868

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.