FDA 510(k) Applications for Medical Device Product Code "GSO"
(Antigens (Febrile), Agglutination, Brucella Spp.)

FDA 510(k) Number Applicant Device Name Decision Date
K972394 LEE LABORATORIES, INC. VISTA ANTIGEN BRUCELLA ABORTUS 08/25/1997
K972396 LEE LABORATORIES, INC. VISTA ANTIGEN BRUCELLA MELITENSIS 08/25/1997


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