K213890 is an FDA 510(k) clearance for the IMICRYL Impression Materials. This device is classified as a Material, Impression (Class II - Special Controls, product code ELW).
Submitted by Imicryl Dis Malzemeleri San. VE Tic. A.S. (Konya, TR). The FDA issued a Cleared decision on February 11, 2022, 60 days after receiving the submission on December 13, 2021.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3660.
| 510(k) Number | K213890 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 13, 2021 |
| Decision Date | February 11, 2022 |
| Days to Decision | 60 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | ELW - Material, Impression |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3660 |