K951583 is an FDA 510(k) clearance for the PERMAQUIK BONDING PRIMER. This device is classified as a Agent, Tooth Bonding, Resin (Class II - Special Controls, product code KLE).
Submitted by Ultradent Products, Inc. (South Jordan, US). The FDA issued a Cleared decision on May 12, 1995, 36 days after receiving the submission on April 6, 1995.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3200.
| 510(k) Number | K951583 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 06, 1995 |
| Decision Date | May 12, 1995 |
| Days to Decision | 36 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Statement |
| Product Code | KLE — Agent, Tooth Bonding, Resin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3200 |