K853002 is an FDA 510(k) clearance for the BISFIL-II(CHEMICAL CURABLE POSTERIOR/ANTERIOR). This device is classified as a Material, Tooth Shade, Resin (Class II - Special Controls, product code EBF).
Submitted by Bisco, Inc. (Lombard, US). The FDA issued a Cleared decision on August 16, 1985, 31 days after receiving the submission on July 16, 1985.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3690.
| 510(k) Number | K853002 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 16, 1985 |
| Decision Date | August 16, 1985 |
| Days to Decision | 31 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 |