ClearanceBrief
510(k) K924070 ยท FMI Needle, Hypodermic, Single Lumen

B-D PEN NEEDLE

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US
DecisionSubstantially Equivalent, Mar 18, 1993
ReceivedAug 12, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924070

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.