ClearanceBrief
510(k) K130049 ยท FMF Syringe, Piston

MONOJECT 12ML SYRINGE

ApplicantNipro Medical Corporation, Miami FL, US
DecisionSubstantially Equivalent, Feb 14, 2013
ReceivedJan 8, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K130049

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.