The following data is part of a premarket notification filed by Chesson Laboratory Associates, Inc. with the FDA for Liquid Bandage.
Device ID | K120059 |
510k Number | K120059 |
Device Name: | LIQUID BANDAGE |
Classification | Bandage, Liquid |
Applicant | CHESSON LABORATORY ASSOCIATES, INC. 603 ELLIS ROAD Durham, NC 27703 |
Contact | Scott E Neuville |
Correspondent | Scott E Neuville CHESSON LABORATORY ASSOCIATES, INC. 603 ELLIS ROAD Durham, NC 27703 |
Product Code | KMF |
CFR Regulation Number | 880.5090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-01-09 |
Decision Date | 2012-05-17 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIQUID BANDAGE 90530052 not registered Live/Pending |
Conopco, Inc. 2021-02-16 |
LIQUID BANDAGE 76398216 2851484 Dead/Cancelled |
JOHNSON & JOHNSON 2002-04-19 |
LIQUID BANDAGE 76398215 2856420 Dead/Cancelled |
JOHNSON & JOHNSON 2002-04-19 |