FDA 510(k) Applications for Medical Device Product Code "CDF"
(Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K953077 | BECKMAN INSTRUMENTS, INC. | PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM | 01/05/1996 |
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