The following data is part of a premarket notification filed by Norcliff Thayer, Inc. with the FDA for Orabrite.
Device ID | K780174 |
510k Number | K780174 |
Device Name: | ORABRITE |
Classification | Cleaner, Denture, Mechanical |
Applicant | NORCLIFF THAYER, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JER |
CFR Regulation Number | 872.3530 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-02-02 |
Decision Date | 1978-02-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ORABRITE 85247526 4361775 Live/Registered |
Oraline, Inc. 2011-02-21 |
ORABRITE 85197473 4283447 Live/Registered |
Oraline, Inc. 2010-12-14 |
ORABRITE 72300574 0873591 Dead/Expired |
FOREMOST-MCKESSON, INC. 1968-06-17 |