CDF — Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin Class I
FDA Device Classification
Classification Details
- Product Code
- CDF
- Device Class
- Class I
- Regulation Number
- 862.1795
- Submission Type
- Review Panel
- CH
- Medical Specialty
- Clinical Chemistry
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K953077 | beckman instruments | PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM | January 5, 1996 |
| K934977 | esa | MODEL 5500 CEAS | January 11, 1994 |
| K895288 | yamasa shoy co | HVA EIA KIT YAMASA | October 31, 1989 |
| K895287 | yamasa shoy co | VMA EIA KIT YAMASA | October 30, 1989 |
| K873372 | bio-rad | HVA & HOMOVANILLIC ACID BY HPLC METHOD | December 22, 1987 |
| K861962 | sterling diagnostics | VANILMANDELIC ACID (VMA) REAGENT SET | July 7, 1986 |
| K861010 | bio-rad | VMA BY HPLC TEST (VANILMANDELIC ACID) | May 1, 1986 |
| K853041 | german american chamber of commerce | TRIGLYCERIDES LCK 124 | August 12, 1985 |
| K843379 | diagnostic chemicals, ltd. (usa) | VMA ASSAY KIT | September 28, 1984 |
| K810992 | helena laboratories | HELENA VMA-SMC COLUMN METHOD | April 29, 1981 |
| K791837 | bio-rad | VMA BY COLUMN TEST | October 30, 1979 |
| K772151 | eppendorf-brinkmann | URINARY VMA - SCREEN TEST KIT | November 30, 1977 |