K780423 is an FDA 510(k) clearance for the STIKSEP-T4 RIA KIT. This device is classified as a Radioimmunoassay, Total Thyroxine (Class II - Special Controls, product code CDX).
Submitted by Nuclear Diagnostics, Inc. (Mchenry, US). The FDA issued a Cleared decision on March 30, 1978, 14 days after receiving the submission on March 16, 1978.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.1700.
| 510(k) Number | K780423 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 16, 1978 |
| Decision Date | March 30, 1978 |
| Days to Decision | 14 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | CDX — Radioimmunoassay, Total Thyroxine |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1700 |