FDA 510(k) Applications for Medical Device Product Code "LGQ"
(Fluorescence Polarization Immunoassay, Phenobarbital)

FDA 510(k) Number Applicant Device Name Decision Date
K972331 OXIS INTL., INC. INNOFLUOR GENTAMICIN ASSAY SYSTEM 08/01/1997
K972330 OXIS INTL., INC. INNOFLUOR PHENOBARBITAL ASSAY SYSTEM 07/14/1997


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