ClearanceBrief
510(k) K821338 ยท GRM Antisera, All Groups, Salmonella Spp.

SALMONELLA I.D.

ApplicantAnalytical Products, Inc., Walker MI, US
DecisionSubstantially Equivalent, May 28, 1982
ReceivedMay 5, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821338

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.