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 |