The following data is part of a premarket notification filed by Parkell, Inc. with the FDA for Brush&bond Plus.
Device ID | K151518 |
510k Number | K151518 |
Device Name: | BRUSH&BOND PLUS |
Classification | Agent, Tooth Bonding, Resin |
Applicant | Parkell, Inc. 300 Executive Drive Edgewood, NY 11717 |
Contact | David Mott |
Correspondent | David Mott Parkell, Inc. 300 Executive Drive Edgewood, NY 11717 |
Product Code | KLE |
CFR Regulation Number | 872.3200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-05 |
Decision Date | 2015-09-18 |
Summary: | summary |