FDA 510(k) Applications Submitted by TOGO Medikit Co., Ltd.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K190001 |
01/02/2019 |
Supercath 5 |
TOGO MEDIKIT Co., Ltd. |
K200379 |
02/18/2020 |
Super Sheath |
TOGO MEDIKIT CO., LTD. |
K160592 |
03/01/2016 |
SUPERCATH 6 |
TOGO MEDIKIT CO., LTD. |
K172496 |
08/18/2017 |
SUPERCATH 5 (26G) |
TOGO Medikit Co., Ltd. |
K081953 |
07/09/2008 |
SUPERCATH 5 |
TOGO MEDIKIT CO., LTD. |
K112290 |
08/09/2011 |
SUPERCATH Z3V |
TOGO MEDIKIT CO., LTD. |
K052267 |
08/19/2005 |
SUPERCATH V |
TOGO MEDIKIT CO., LTD. |
K093546 |
11/17/2009 |
SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX |
TOGO MEDIKIT CO., LTD. |
K121504 |
05/21/2012 |
SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS |
TOGO MEDIKIT CO., LTD. |
K060190 |
01/24/2006 |
SUPER SHEATH XL INTRODUCER SHEATH |
TOGO MEDIKIT CO., LTD. |
K052557 |
09/16/2005 |
SUPER SHEATH INTRODUCER SHEATH |
TOGO MEDIKIT CO., LTD. |
K140419 |
02/18/2014 |
SUPERCATH5 |
TOGO MEDIKIT CO., LTD. |
K141070 |
04/25/2014 |
SUPER SHEATH |
TOGO MEDIKIT CO., LTD. |
K050114 |
01/18/2005 |
SUPERCATH Z3V |
TOGO MEDIKIT CO., LTD. |
|
|