The following data is part of a premarket notification filed by Togard, Inc. with the FDA for Toguard.
Device ID | K790652 |
510k Number | K790652 |
Device Name: | TOGUARD |
Classification | Shoe, Cast |
Applicant | TOGARD, INC. 803 N. Front St. Suite 3 McHenry, IL 60050 |
Product Code | IPG |
CFR Regulation Number | 890.3025 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-04-04 |
Decision Date | 1979-04-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TOGUARD 86750782 4941141 Live/Registered |
Shenzhen Jingmai trade CO., Limited 2015-09-09 |