ClearanceBrief
510(k) K993666 ยท FMF Syringe, Piston

DISETRONIC PEN P100

ApplicantDisetronic Medical Systems, Fort Myers FL, US
DecisionSubstantially Equivalent, Nov 22, 1999
ReceivedNov 1, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K993666

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.