The following data is part of a premarket notification filed by Hycel, Inc. with the FDA for Direct Urea Nitrogen Test.
| Device ID | K780262 |
| 510k Number | K780262 |
| Device Name: | DIRECT UREA NITROGEN TEST |
| Classification | Diacetyl-monoxime, Urea Nitrogen |
| Applicant | HYCEL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CDW |
| CFR Regulation Number | 862.1770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-02-17 |
| Decision Date | 1978-04-05 |