K801475 is an FDA 510(k) clearance for the APPLICATION OF EMIT AED ASSAYS. This device is classified as a Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine (Class II - Special Controls, product code KLI).
Submitted by Syva Co. (Mchenry, US). The FDA issued a Cleared decision on July 8, 1980, 14 days after receiving the submission on June 24, 1980.
This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.1700.
| 510(k) Number | K801475 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 24, 1980 |
| Decision Date | July 08, 1980 |
| Days to Decision | 14 days |
| Submission Type | Traditional |
| Review Panel | Toxicology (TX) |
| Summary | — |
| Product Code | KLI — Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1700 |