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  |