ClearanceBrief
510(k) K821100 ยท GTZ Antisera, All Groups, Streptococcus Spp.

MERITECASTREP (TM)

ApplicantMeridian Diagnostics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 13, 1982
ReceivedApr 20, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821100

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.