K802969 is an FDA 510(k) clearance for the CORTISOL 125-I RADIOIMMUNOASSAY KIT. This device is classified as a Radioimmunoassay, Cortisol (Class II - Special Controls, product code CGR).
Submitted by Ria Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 2, 1981, 42 days after receiving the submission on November 21, 1980.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1205.
| 510(k) Number | K802969 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 21, 1980 |
| Decision Date | January 02, 1981 |
| Days to Decision | 42 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | CGR — Radioimmunoassay, Cortisol |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1205 |