Togo Medikit Co., Ltd.

FDA Regulatory Profile

Togo Medikit Co., Ltd. appears in FDA public data with 0 recalls, 17 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 17, 2024.

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-3W7/1008Sep 17, 2024
K200379Super SheathMar 19, 2020
K190001Supercath 5Sep 20, 2019
K172496SUPERCATH 5 (26G)Mar 23, 2018
K160592SUPERCATH 6Aug 12, 2016
K141070SUPER SHEATHJan 15, 2015
K140419SUPERCATH5May 12, 2014
K121504SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETSSep 27, 2012
K112290SUPERCATH Z3VApr 16, 2012
K093546SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XXDec 17, 2009
K081953SUPERCATH 5Mar 12, 2009
K052267SUPERCATH VOct 27, 2006
K060190SUPER SHEATH XL INTRODUCER SHEATHApr 4, 2006
K052557SUPER SHEATH INTRODUCER SHEATHJan 17, 2006
K050114SUPERCATH Z3VJun 9, 2005
K864038SUPERCATH I.V. CATHETERDec 4, 1986
K854773SUPERCATH A.V. FISTULAApr 8, 1986