K881918 is an FDA 510(k) clearance for the LIGHT-CURED ZIONOMER CEMENT. This device is classified as a Cement, Dental (Class II - Special Controls, product code EMA).
Submitted by Den-Mat Corp. (Santa Maria, US). The FDA issued a Cleared decision on July 15, 1988, 67 days after receiving the submission on May 9, 1988.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3275.
| 510(k) Number | K881918 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 09, 1988 |
| Decision Date | July 15, 1988 |
| Days to Decision | 67 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EMA — Cement, Dental |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3275 |