The following data is part of a premarket notification filed by Diagnon Corp. with the FDA for Diagnon B12 57co Ria Kit.
| Device ID | K832717 |
| 510k Number | K832717 |
| Device Name: | DIAGNON B12 57CO RIA KIT |
| Classification | Radioassay, Vitamin B12 |
| Applicant | DIAGNON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CDD |
| CFR Regulation Number | 862.1810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-08-12 |
| Decision Date | 1983-12-08 |