The following data is part of a premarket notification filed by Synermed, Inc. with the FDA for Synermed Uric Acid Reagent Kit.
| Device ID | K903727 |
| 510k Number | K903727 |
| Device Name: | SYNERMED URIC ACID REAGENT KIT |
| Classification | Acid, Uric, Uricase (colorimetric) |
| Applicant | SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Contact | Marcia J Arentz |
| Correspondent | Marcia J Arentz SYNERMED, INC. 1688 50TH AVENUE, MONTREAL (LACHINE), Quebec, Canada, CA H8t 2v5 |
| Product Code | KNK |
| CFR Regulation Number | 862.1775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-08-16 |
| Decision Date | 1990-09-27 |