510(k) K791837

VMA BY COLUMN TEST by Bio-Rad — Product Code CDF

K791837 is an FDA 510(k) premarket notification submitted by Bio-Rad for the device "VMA BY COLUMN TEST". The FDA issued a decision of Substantially Equivalent on October 30, 1979. The device falls under product code CDF (Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin), a Class I device regulated under 21 CFR 862.1795. Bio-Rad has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 30, 1979
Date Received
September 14, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin
Device Class
Class I
Regulation Number
862.1795
Review Panel
CH
Submission Type