K192586 is an FDA 510(k) clearance for the LIAISON® Folate. This device is classified as a Acid, Folic, Radioimmunoassay (Class II - Special Controls, product code CGN).
Submitted by DiaSorin, Inc. (Stillwater, US). The FDA issued a Cleared decision on May 6, 2020, 230 days after receiving the submission on September 19, 2019.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1295.
| 510(k) Number | K192586 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 19, 2019 |
| Decision Date | May 06, 2020 |
| Days to Decision | 230 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CGN — Acid, Folic, Radioimmunoassay |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 862.1295 |