K890140 is an FDA 510(k) clearance for the PHOSPHORIC-ACID ETCHING GEL. This device is classified as a Material, Tooth Shade, Resin (Class II - Special Controls, product code EBF).
Submitted by Centrix, Inc. (Milford, US). The FDA issued a Cleared decision on March 29, 1989, 75 days after receiving the submission on January 13, 1989.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3690.
| 510(k) Number | K890140 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 13, 1989 |
| Decision Date | March 29, 1989 |
| Days to Decision | 75 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | — |
| Product Code | EBF — Material, Tooth Shade, Resin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3690 |