ClearanceBrief
510(k) K791571 ยท GLZ Antigens, If, Toxoplasma Gondii

TOXOPLASMA ANTIBODY TEST SYSTEM

ApplicantZeus Scientific, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 24, 1979
ReceivedAug 13, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K791571

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.