The following data is part of a premarket notification filed by Nuclear Diagnostics, Inc. with the FDA for Ria Diag. Test Kit For Indexing Thyrox..
| Device ID | K781560 |
| 510k Number | K781560 |
| Device Name: | RIA DIAG. TEST KIT FOR INDEXING THYROX. |
| Classification | Radioimmunoassay, Free Thyroxine |
| Applicant | NUCLEAR DIAGNOSTICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CEC |
| CFR Regulation Number | 862.1695 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-09-11 |
| Decision Date | 1978-10-17 |