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 |