The following data is part of a premarket notification filed by American Monitor Corp. with the FDA for Activated Uric Acid.
| Device ID | K830616 |
| 510k Number | K830616 |
| Device Name: | ACTIVATED URIC ACID |
| Classification | Acid, Ferric Ion-sulfuric, Cholesterol |
| Applicant | AMERICAN MONITOR CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CHD |
| CFR Regulation Number | 862.1175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-28 |
| Decision Date | 1983-04-05 |