K823317 is an FDA 510(k) clearance for the DENTAL INSTRUMENTS - EXPLORERS..
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.
| 510(k) Number | K823317 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 | — |
| Device Class | — |