K023727 is an FDA 510(k) clearance for the TEMPORARY CEMENT-DC010002. This device is classified as a Cement, Dental (Class II - Special Controls, product code EMA).
Submitted by GC America, Inc. (Alsip, US). The FDA issued a Cleared decision on January 16, 2003, 71 days after receiving the submission on November 6, 2002.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3275.
| 510(k) Number | K023727 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 06, 2002 |
| Decision Date | January 16, 2003 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | EMA — Cement, Dental |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3275 |