ClearanceBrief
510(k) K903945 ยท FIE Needle, Fistula

EXEL A-V FISTULA SET

ApplicantExel Intl., Culver City CA, US
DecisionSubstantially Equivalent, Nov 20, 1990
ReceivedAug 27, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903945

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.