The following data is part of a premarket notification filed by Gamma Enterprises, Inc. with the FDA for Uric Acid.
| Device ID | K771842 |
| 510k Number | K771842 |
| Device Name: | URIC ACID |
| Classification | Acid, Uric, Phosphotungstate Reduction |
| Applicant | GAMMA ENTERPRISES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CDH |
| CFR Regulation Number | 862.1775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-09-21 |
| Decision Date | 1977-10-25 |