ClearanceBrief
510(k) K221974 ยท FMF Syringe, Piston

EpiFinder

ApplicantOmeq Medical , Ltd., Misgav, IL
DecisionSubstantially Equivalent, Apr 16, 2023
ReceivedJul 5, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221974

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.