K023649 is an FDA 510(k) clearance for the VITIQUE SYSTEM. This device is classified as a Cement, Dental (Class II - Special Controls, product code EMA).
Submitted by Dmg USA, Inc. (Ayer, US). The FDA issued a Cleared decision on January 17, 2003, 79 days after receiving the submission on October 30, 2002.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3275.
| 510(k) Number | K023649 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 30, 2002 |
| Decision Date | January 17, 2003 |
| Days to Decision | 79 days |
| Submission Type | Abbreviated |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EMA — Cement, Dental |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3275 |