ClearanceBrief
510(k) K832658 ยท FMF Syringe, Piston

DIRECTOR

ApplicantPharmacia, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 4, 1983
ReceivedAug 8, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832658

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.