K781281 is an FDA 510(k) clearance for the CEMENT, DENTAL/CAVITY LINER. This device is classified as a Cement, Dental (Class II - Special Controls, product code EMA).
Submitted by Star Dental Mfg. Co. (Mchenry, US). The FDA issued a Cleared decision on August 21, 1978, 26 days after receiving the submission on July 26, 1978.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3275.
| 510(k) Number | K781281 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 26, 1978 |
| Decision Date | August 21, 1978 |
| Days to Decision | 26 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 |