The following data is part of a premarket notification filed by Seragen Diagnostics, Inc. with the FDA for Urea Nitrogen-uv.
| Device ID | K833931 |
| 510k Number | K833931 |
| Device Name: | UREA NITROGEN-UV |
| Classification | Urease And Glutamic Dehydrogenase, Urea Nitrogen |
| Applicant | SERAGEN DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CDQ |
| CFR Regulation Number | 862.1770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-11-14 |
| Decision Date | 1984-01-13 |