The following data is part of a premarket notification filed by Dmg Usa, Inc. with the FDA for Dental Ceramic.
| Device ID | K080479 |
| 510k Number | K080479 |
| Device Name: | DENTAL CERAMIC |
| Classification | Powder, Porcelain |
| Applicant | DMG USA, INC. 5 WHITCOMB AVE. Ayer, MA 01432 |
| Contact | Pamela Papineau |
| Correspondent | Pamela Papineau DMG USA, INC. 5 WHITCOMB AVE. Ayer, MA 01432 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-02-22 |
| Decision Date | 2008-05-21 |
| Summary: | summary |