FDA 510(k) Applications for Medical Device Product Code "JPZ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K020486 | CARESIDE, INC. | CARESIDE GGT | 07/01/2002 |
K961919 | DATA MEDICAL ASSOCIATES, INC. | DMA GAMMA GLUTAMYLTRANSFERASE (GGT) PROCEDURE | 07/01/1996 |