ClearanceBrief
510(k) K930342 ยท FMF Syringe, Piston

BECTON DICKINSON ARTERIAL BLOOD GAS KITS

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US
DecisionSubstantially Equivalent, Apr 7, 1993
ReceivedJan 25, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K930342

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.