The following data is part of a premarket notification filed by Gilford Diagnostics with the FDA for Triglyceride Reagent (uv).
| Device ID | K823709 |
| 510k Number | K823709 |
| Device Name: | TRIGLYCERIDE REAGENT (UV) |
| Classification | Lipase Hydrolysis/glycerol Kinase Enzyme, Triglycerides |
| Applicant | GILFORD DIAGNOSTICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CDT |
| CFR Regulation Number | 862.1705 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-09 |
| Decision Date | 1983-01-07 |