K897020 is an FDA 510(k) clearance for the ALL-BOND DENTIN BONDING SYSTEM. This device is classified as a Agent, Tooth Bonding, Resin (Class II - Special Controls, product code KLE).
Submitted by Bisco, Inc. (Downers Grove, US). The FDA issued a Cleared decision on March 14, 1990, 85 days after receiving the submission on December 19, 1989.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3200.
| 510(k) Number | K897020 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 19, 1989 |
| Decision Date | March 14, 1990 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | KLE — Agent, Tooth Bonding, Resin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3200 |