The following data is part of a premarket notification filed by Syn-kit, Inc. with the FDA for Uricase (u.v.) Uric Acid.
| Device ID | K821167 |
| 510k Number | K821167 |
| Device Name: | URICASE (U.V.) URIC ACID |
| Classification | Acid, Uric, Uricase (u.v.) |
| Applicant | SYN-KIT, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CDO |
| CFR Regulation Number | 862.1775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-04-27 |
| Decision Date | 1982-05-14 |