The following data is part of a premarket notification filed by Boehringer Mannheim Corp. with the FDA for Bun (kinetic).
| Device ID | K895666 |
| 510k Number | K895666 |
| Device Name: | BUN (KINETIC) |
| Classification | Urease And Glutamic Dehydrogenase, Urea Nitrogen |
| Applicant | BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Contact | Cheri Emmons |
| Correspondent | Cheri Emmons BOEHRINGER MANNHEIM CORP. 9115 HAGUE RD. Indianapolis, IN 46250 -0457 |
| Product Code | CDQ |
| CFR Regulation Number | 862.1770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-09-20 |
| Decision Date | 1989-10-27 |