K953344 is an FDA 510(k) clearance for the DEGUBOND ULTRA. This device is classified as a Alloy, Gold-based Noble Metal (Class II - Special Controls, product code EJT).
Submitted by Degussa AG (South Plainfield, US). The FDA issued a Cleared decision on August 25, 1995, 44 days after receiving the submission on July 12, 1995.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3060.
| 510(k) Number | K953344 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 12, 1995 |
| Decision Date | August 25, 1995 |
| Days to Decision | 44 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EJT — Alloy, Gold-based Noble Metal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3060 |