ClearanceBrief
510(k) K855233 ยท GTN Antisera, Fluorescent, All Types, Staphylococcus Spp.

DIAGNOSTIC REAGENT SET-RPLA

ApplicantOxoid U.S.A., Inc., Columbia MD, US
DecisionSubstantially Equivalent, Nov 4, 1986
ReceivedDec 31, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K855233

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.