Submission Details
| 510(k) Number | K954362 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 18, 1995 |
| Decision Date | October 12, 1995 |
| Days to Decision | 24 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
K954362 is an FDA 510(k) clearance for the ARGISTAR 74, 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 12, 1995, 24 days after receiving the submission on September 18, 1995. This device falls under the Dental review panel. Regulated under 21 CFR 872.3060.
| 510(k) Number | K954362 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 18, 1995 |
| Decision Date | October 12, 1995 |
| Days to Decision | 24 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 |