The following data is part of a premarket notification filed by Seragen Diagnostics, Inc. with the FDA for Seragan Acth125 I-ria Kit.
| Device ID | K822115 |
| 510k Number | K822115 |
| Device Name: | SERAGAN ACTH125 I-RIA KIT |
| Classification | Radioimmunoassay, Acth |
| Applicant | SERAGEN DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CKG |
| CFR Regulation Number | 862.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-07-19 |
| Decision Date | 1982-10-18 |