The following data is part of a premarket notification filed by Ivoclar Vivadent, Inc. with the FDA for Bluephase Style.
Device ID | K110756 |
510k Number | K110756 |
Device Name: | BLUEPHASE STYLE |
Classification | Activator, Ultraviolet, For Polymerization |
Applicant | IVOCLAR VIVADENT, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
Contact | Donna Marie Hartnett |
Correspondent | Donna Marie Hartnett IVOCLAR VIVADENT, INC. 175 PINEVIEW DR. Amherst, NY 14228 |
Product Code | EBZ |
CFR Regulation Number | 872.6070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-03-18 |
Decision Date | 2011-08-29 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BLUEPHASE STYLE 85241212 4199358 Live/Registered |
Ivoclar Vivadent, Inc. 2011-02-14 |