ClearanceBrief
510(k) K212677 ยท FMF Syringe, Piston

aboNT SYRINGE

ApplicantNipro Medical Corporation, Miami FL, US
DecisionSubstantially Equivalent, Apr 15, 2022
ReceivedAug 24, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212677

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.