510(k) K791837
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