ClearanceBrief
510(k) K810510 ยท GMD Antisera, Latex Agglutination, Cryptococcus Neoformans

YA-CRYPTO ANTIBODY TUBE AGGLUTINATION

ApplicantImmuno-Mycologics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 20, 1981
ReceivedFeb 24, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810510

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.