ClearanceBrief
510(k) K212544 ยท FMF Syringe, Piston

MiniLoad Syringe

ApplicantOcuject, LLC, Newport Beach CA, US
DecisionSubstantially Equivalent, Oct 13, 2021
ReceivedAug 12, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K212544

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.