K862871 is an FDA 510(k) clearance for the RADIOIMMUNOASSAY OF NO SPIN(TM) CORTISOL. This device is classified as a Radioimmunoassay, Cortisol (Class II - Special Controls, product code CGR).
Submitted by Cambridge Medical Technology (Billerica, US). The FDA issued a Cleared decision on August 19, 1986, 21 days after receiving the submission on July 29, 1986.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1205.
| 510(k) Number | K862871 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 29, 1986 |
| Decision Date | August 19, 1986 |
| Days to Decision | 21 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 |