K242505 is an FDA 510(k) clearance for the Elecsys Cortisol III. This device is classified as a Fluorometric, Cortisol (Class II - Special Controls, product code JFT).
Submitted by Roche Diagnostics (Indianapolis, US). The FDA issued a Cleared decision on July 17, 2025, 329 days after receiving the submission on August 22, 2024.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1205.
| 510(k) Number | K242505 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 22, 2024 |
| Decision Date | July 17, 2025 |
| Days to Decision | 329 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | JFT — Fluorometric, Cortisol |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1205 |