The following data is part of a premarket notification filed by Catachem, Inc. with the FDA for Bun-blood Urea Nitrogen For Manual/auto Applicat.
| Device ID | K894173 |
| 510k Number | K894173 |
| Device Name: | BUN-BLOOD UREA NITROGEN FOR MANUAL/AUTO APPLICAT |
| Classification | Urease And Glutamic Dehydrogenase, Urea Nitrogen |
| Applicant | CATACHEM, INC. 6 NORTH PEARL ST. Port Chester, NY 10573 |
| Contact | Luis P Leon |
| Correspondent | Luis P Leon CATACHEM, INC. 6 NORTH PEARL ST. Port Chester, NY 10573 |
| Product Code | CDQ |
| CFR Regulation Number | 862.1770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-06-15 |
| Decision Date | 1989-09-05 |