Vma by Column Test
by Bio-Rad
510(k) K791837
Vma by Column Test is a medical device (FDA Class I; FDA product code CDF, Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin) made by Bio-Rad, cleared under FDA 510(k) K791837 on 30 Oct 1979, active as of 11 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK791837 | Date30 Oct 1979 | StatusActive |
Official records
- FDA 510(k) database K791837
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- CDF
- Device class
- Class I
- Regulation
- 21 CFR Part 862.1795
- Advisory committee
- Clinical Chemistry
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code CDF (Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin).
- MODEL 5500 CEAS by Esa, Inc.
- Reagent Kit 80800/480 by Chromsystems Instruments & Chemicals GmbH
- Reagent 80804 by Chromsystems Instruments & Chemicals GmbH
- URINARY VMA - SCREEN TEST KIT by Eppendorf-Brinkmann, Inc.
- HELENA VMA-SMC COLUMN METHOD by Helena Laboratories, Corp.
- VANILMANDELIC ACID (VMA) REAGENT SET by STERLING DIAGNOSTICS INC
- TRIGLYCERIDES LCK 124 by German American Chamber of Commerce, Inc.
- VMA EIA KIT YAMASA by Yamasa Shoy Co., Ltd.
- PARAGON CZE 2000 CLINICAL CAPILLARY ELECTROPHORESIS SYSTEM by Beckman Instruments, Inc.
- VMA ASSAY KIT by Diagnostic Chemicals, Ltd. (Usa)