ClearanceBrief
510(k) K992351 ยท FMF Syringe, Piston

SEALOUETTE FIBRIN SEALANT APPLICATOR

ApplicantBiosurgical Corp., Pleasanton CA, US
DecisionSubstantially Equivalent, Oct 8, 1999
ReceivedJul 14, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K992351

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.