FDA 510(k) Applications for Medical Device Product Code "LGQ"
|
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 |