FDA 510(k) Applications for Medical Device Product Code "JGQ"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K981295 | ABBOTT LABORATORIES | UPRO | 10/01/1998 |
K981682 | ABBOTT LABORATORIES | UPRO | 09/21/1998 |
K131051 | HITACHI CHEMICAL DIAGNOSTICS, INC. | HITACHI S TEST REAGENT CARTRIDGE TOTAL PROTEIN (TP) AND ALBUMIN (ALB) | 06/07/2013 |
K071239 | Roche Diagnostics | TOTAL PROTEIN URINE/CSF GEN.3 | 09/14/2007 |
K072638 | ROCHE DIAGNOSTICS CORP. | ROCHE/HITACHI URINARY/CSF PROTEIN WITH MODEL(S) CAT #11877801 | 10/19/2007 |