Submission Details
| 510(k) Number | K954371 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 19, 1995 |
| Decision Date | October 07, 1995 |
| Days to Decision | 18 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
K954371 is an FDA 510(k) clearance for the SUREFIRE S, a Alloy, Gold-based Noble Metal (Class II — Special Controls, product code EJT), submitted by Argen Precious Metals, Inc. (San Diego, US). The FDA issued a Cleared decision on October 7, 1995, 18 days after receiving the submission on September 19, 1995. This device falls under the Dental review panel. Regulated under 21 CFR 872.3060.
| 510(k) Number | K954371 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 19, 1995 |
| Decision Date | October 07, 1995 |
| Days to Decision | 18 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | EJT — Alloy, Gold-based Noble Metal |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 872.3060 |