The following data is part of a premarket notification filed by Fisher Scientific Co., Llc. with the FDA for Bun Reagent Kit.
| Device ID | K800071 |
| 510k Number | K800071 |
| Device Name: | BUN REAGENT KIT |
| Classification | Electrode, Ion Specific, Urea Nitrogen |
| Applicant | FISHER SCIENTIFIC CO., LLC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CDS |
| CFR Regulation Number | 862.1770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-01-11 |
| Decision Date | 1980-02-05 |