K823323 is an FDA 510(k) clearance for the DENTAL INSTRUMENTS - PLASTIC INSTRUMENTS. This device is classified as a Instrument, Filling, Plastic, Dental (Class I - General Controls, product code EIY).
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 | K823323 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (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 | EIY — Instrument, Filling, Plastic, Dental |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 872.4565 |