ClearanceBrief
510(k) K881457 ยท GTZ Antisera, All Groups, Streptococcus Spp.

KODAK SURECELL STREP A TEST KIT

ApplicantEastman Kodak Company, Rochester NY, US
DecisionSubstantially Equivalent, Apr 21, 1988
ReceivedApr 6, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881457

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.