Submission Details
| 510(k) Number | K823315 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 08, 1982 |
| Decision Date | November 24, 1982 |
| Days to Decision | 16 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
K823315 is an FDA 510(k) clearance for the DENTAL INSTRUMENTS - KNIVES. This device is classified as a Knife, Margin Finishing, Operative (Class I — General Controls, product code EJZ).
Submitted by Miltex, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 24, 1982, 16 days after receiving the submission on November 8, 1982.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.4565.
| 510(k) Number | K823315 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 08, 1982 |
| Decision Date | November 24, 1982 |
| Days to Decision | 16 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EJZ — Knife, Margin Finishing, Operative |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 872.4565 |