ClearanceBrief
510(k) K203738 ยท FMF Syringe, Piston

Qitexio

ApplicantMedex, Saint-Priest, FR
DecisionSubstantially Equivalent, Mar 14, 2022
ReceivedDec 22, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203738

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.