ClearanceBrief
510(k) K792681 ยท KFH Antiserum, Positive Control, Blastomyces Dermatitidis

BLASTOMYCES DERMATITIDIS POS/CONTROL

ApplicantMeridian Diagnostics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 17, 1980
ReceivedDec 27, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792681

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.