ClearanceBrief
510(k) K002381 ยท FMF Syringe, Piston

PENTAFERTE SINGLE USE SYRINGES, MODEL SIZE=VARIOUS SIZES

ApplicantPentaferte, S.R.L., Campli (Teramo), IT
DecisionSubstantially Equivalent, Jan 11, 2001
ReceivedAug 4, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002381

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.