The following data is part of a premarket notification filed by Gilford Diagnostics with the FDA for Creatinine Reagent.
| Device ID | K811659 |
| 510k Number | K811659 |
| Device Name: | CREATININE REAGENT |
| Classification | Alkaline Picrate, Colorimetry, Creatinine |
| Applicant | GILFORD DIAGNOSTICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CGX |
| CFR Regulation Number | 862.1225 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-06-12 |
| Decision Date | 1981-06-26 |