K062409 is an FDA 510(k) clearance for the K-ETCHANT GEL. This device is classified as a Material, Tooth Shade, Resin (Class II — Special Controls, product code EBF).
Submitted by Kuraray Medical, Inc. (New York, US). The FDA issued a Cleared decision on November 8, 2006, 83 days after receiving the submission on August 17, 2006.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3690.
| 510(k) Number | K062409 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 17, 2006 |
| Decision Date | November 08, 2006 |
| Days to Decision | 83 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EBF — Material, Tooth Shade, Resin |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3690 |