The following data is part of a premarket notification filed by Voco Gmbh with the FDA for Grandio Flow.
Device ID | K101213 |
510k Number | K101213 |
Device Name: | GRANDIO FLOW |
Classification | Material, Tooth Shade, Resin |
Applicant | VOCO GMBH ANTON-FLETTNER-STRASSE 1-3 Cuxhaven, DE D-27472 |
Contact | M Plaumann |
Correspondent | M Plaumann VOCO GMBH ANTON-FLETTNER-STRASSE 1-3 Cuxhaven, DE D-27472 |
Product Code | EBF |
CFR Regulation Number | 872.3690 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-04-30 |
Decision Date | 2010-08-19 |