K955647 is an FDA 510(k) clearance for the VIDAS ESTRADIOL II (E2II) ASSAY. This device is classified as a Radioimmunoassay, Estradiol (Class I - General Controls, product code CHP).
Submitted by Biomerieux Vitek, Inc. (Rockland, US). The FDA issued a Cleared decision on February 6, 1996, 56 days after receiving the submission on December 12, 1995.
This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1260.
| 510(k) Number | K955647 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 12, 1995 |
| Decision Date | February 06, 1996 |
| Days to Decision | 56 days |
| Submission Type | Traditional |
| Review Panel | Chemistry (CH) |
| Summary | Summary PDF |
| Product Code | CHP — Radioimmunoassay, Estradiol |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 862.1260 |