ClearanceBrief
510(k) K262242 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

Profoject™ Safe Push Button Blood Collection Sets

ApplicantCMT Health PTE., Ltd., Singapore, SG
DecisionSubstantially Equivalent, Oct 28, 2026
ReceivedJul 1, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K262242

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.