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Togo Medikit Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241230Super Sheath Introducer Sheath S-3N5/1005 S-3N7/1006 S-3W5/1007 S-3W7/1008September 17, 2024
K200379Super SheathMarch 19, 2020
K190001Supercath 5September 20, 2019
K172496SUPERCATH 5 (26G)March 23, 2018
K160592SUPERCATH 6August 12, 2016
K141070SUPER SHEATHJanuary 15, 2015
K140419SUPERCATH5May 12, 2014
K121504SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETSSeptember 27, 2012
K112290SUPERCATH Z3VApril 16, 2012
K093546SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XXDecember 17, 2009
K081953SUPERCATH 5March 12, 2009
K052267SUPERCATH VOctober 27, 2006
K060190SUPER SHEATH XL INTRODUCER SHEATHApril 4, 2006
K052557SUPER SHEATH INTRODUCER SHEATHJanuary 17, 2006
K050114SUPERCATH Z3VJune 9, 2005
K864038SUPERCATH I.V. CATHETERDecember 4, 1986
K854773SUPERCATH A.V. FISTULAApril 8, 1986