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