K950299 is an FDA 510(k) clearance for the CEREC 2. This device is classified as a Material, Impression (Class II - Special Controls, product code ELW).
Submitted by Pelton & Crane Co. (Charlotte, US). The FDA issued a Cleared decision on May 23, 1995, 118 days after receiving the submission on January 25, 1995.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3660.
| 510(k) Number | K950299 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 25, 1995 |
| Decision Date | May 23, 1995 |
| Days to Decision | 118 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | ELW — Material, Impression |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3660 |