The following data is part of a premarket notification filed by Dermadry Laboratories Inc. with the FDA for Dermadry.
Device ID | K192749 |
510k Number | K192749 |
Device Name: | Dermadry |
Classification | Device, Iontophoresis, Other Uses |
Applicant | Dermadry Laboratories Inc. 9223 Langelier Blvd Montreal, CA H1p 3k9 |
Contact | Maxime Calouche |
Correspondent | Louis-paul Marin LOK North America Inc. 2025 Michelin Street Laval, CA H7l5b7 |
Product Code | EGJ |
CFR Regulation Number | 890.5525 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-09-30 |
Decision Date | 2020-02-10 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00877067000034 | K192749 | 000 |
00877067000027 | K192749 | 000 |
00877067000010 | K192749 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DERMADRY 88148595 not registered Live/Pending |
Associated Hygienic Products LLC 2018-10-09 |
DERMADRY 87571859 5676107 Live/Registered |
DERMADRY LABORATORIES INC. 2017-08-16 |
DERMADRY 86926212 5282065 Live/Registered |
Attends Healthcare Products, Inc. 2016-03-02 |
DERMADRY 86921751 5031995 Live/Registered |
Attends Healthcare Products, Inc. 2016-02-26 |
DERMADRY 78568491 not registered Dead/Abandoned |
Consumer Care of America, LLC 2005-02-16 |