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 |