The following data is part of a premarket notification filed by Axiom, Inc. with the FDA for Axiom Stable Ii Uric Acid Test.
| Device ID | K842442 |
| 510k Number | K842442 |
| Device Name: | AXIOM STABLE II URIC ACID TEST |
| Classification | Acid, Uric, Uricase (colorimetric) |
| Applicant | AXIOM, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KNK |
| CFR Regulation Number | 862.1775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-06-21 |
| Decision Date | 1984-08-16 |