The following data is part of a premarket notification filed by E. R. Squibb & Sons, Inc. with the FDA for T4-squibb Ria Kit.
| Device ID | K802456 |
| 510k Number | K802456 |
| Device Name: | T4-SQUIBB RIA KIT |
| Classification | Radioimmunoassay, Total Thyroxine |
| Applicant | E. R. SQUIBB & SONS, INC. GEORGES RD. New Brunswick, NJ |
| Product Code | CDX |
| CFR Regulation Number | 862.1700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-10-08 |
| Decision Date | 1980-10-31 |