K854419 is an FDA 510(k) clearance for the TDX CORTISOL. This device is classified as a Fluorometric, Cortisol (Class II - Special Controls, product code JFT).
Submitted by Abbott Laboratories (Abbott Park, US). The FDA issued a Cleared decision on November 25, 1985, 21 days after receiving the submission on November 4, 1985.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1205.
| 510(k) Number | K854419 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 04, 1985 |
| Decision Date | November 25, 1985 |
| Days to Decision | 21 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | — |
| Product Code | JFT — Fluorometric, Cortisol |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1205 |