The following data is part of a premarket notification filed by Vita Zahnfabrik H. Rauter Gmbh & Co. Kg. with the FDA for Vita Vmk Master.
| Device ID | K093446 |
| 510k Number | K093446 |
| Device Name: | VITA VMK MASTER |
| Classification | Powder, Porcelain |
| Applicant | VITA ZAHNFABRIK H. RAUTER GMBH & CO. KG. 3150 EAST BIRCH ST. Brea, CA 92821 |
| Contact | Elizabeth Wolfsen |
| Correspondent | Elizabeth Wolfsen VITA ZAHNFABRIK H. RAUTER GMBH & CO. KG. 3150 EAST BIRCH ST. Brea, CA 92821 |
| Product Code | EIH |
| CFR Regulation Number | 872.6660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-11-05 |
| Decision Date | 2009-12-03 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| J017BVMKSETPCV10 | K093446 | 000 |
| J017BVMKSETP3DV10 | K093446 | 000 |
| J017BVMKSETCV10 | K093446 | 000 |
| J017BVMKSET3DV10 | K093446 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VITA VMK MASTER 76676089 3433731 Live/Registered |
Vita Zahnfabrik H. Rauter GmbH & Co. K.G. 2007-04-27 |