The following data is part of a premarket notification filed by Togo Medikit Co., Ltd. with the FDA for Super Sheath.
| Device ID | K141070 |
| 510k Number | K141070 |
| Device Name: | SUPER SHEATH |
| Classification | Dilator, Vessel, For Percutaneous Catheterization |
| Applicant | TOGO MEDIKIT CO., LTD. 4-1-17 HONGO Bunkyo-ku, JP 113-0033 |
| Contact | Izumi Maruo |
| Correspondent | Izumi Maruo TOGO MEDIKIT CO., LTD. 4-1-17 HONGO Bunkyo-ku, JP 113-0033 |
| Product Code | DRE |
| CFR Regulation Number | 870.1310 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-25 |
| Decision Date | 2015-01-15 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SUPER SHEATH 78696177 3354633 Live/Registered |
MEDIKIT CO., LTD. 2005-08-19 |
![]() SUPER SHEATH 73124775 1093014 Dead/Expired |
HOLLAND PLASTICS, INC. 1977-04-29 |