ClearanceBrief
510(k) K230391 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

BD MiniDraw™ Capillary Blood Collection System with BD MiniDraw™ SST™ Capillary Blood Collection Tube

ApplicantBecton, Dickinson and Company, Franklin Lakes NJ, US
DecisionSubstantially Equivalent, Dec 1, 2023
ReceivedFeb 14, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230391

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.