K013571 is an FDA 510(k) clearance for the MAGICFIL. This device is classified as a Material, Tooth Shade, Resin (Class II - Special Controls, product code EBF).
Submitted by Dmg USA, Inc. (Ayer, US). The FDA issued a Cleared decision on January 17, 2002, 80 days after receiving the submission on October 29, 2001.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3690.
| 510(k) Number | K013571 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 29, 2001 |
| Decision Date | January 17, 2002 |
| Days to Decision | 80 days |
| Submission Type | Abbreviated |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | EBF — Material, Tooth Shade, Resin |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3690 |