ClearanceBrief
510(k) K251812 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

Steripath® Flow™ Blood Collection System

ApplicantMagnolia Medical Technologies, Seattle WA, US
DecisionSubstantially Equivalent, Sep 25, 2025
ReceivedJun 12, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K251812

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.