Togo Medikit Co., Ltd.

17 FDA 510(k) medical device clearances.

Top product codes for Togo Medikit Co., Ltd.

FOZ — General Hospital 9 devices
DRE — Cardiovascular 3 devices
DYB — Cardiovascular 3 devices
FIE — Gastroenterology, Urology 2 devices

Recent clearances by Togo Medikit Co., Ltd.

K241230 — Super Sheath Introducer Sheath S-3N5/1005 S-3N7/1006 S-3W5/1007 S-3W7/1008 DYB · 2024-09-17
K200379 — Super Sheath DRE · 2020-03-19
K190001 — Supercath 5 FOZ · 2019-09-20
K172496 — SUPERCATH 5 (26G) FOZ · 2018-03-23
K160592 — SUPERCATH 6 FOZ · 2016-08-12
K141070 — SUPER SHEATH DRE · 2015-01-15
K140419 — SUPERCATH5 FOZ · 2014-05-12
K121504 — SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS DYB · 2012-09-27
K112290 — SUPERCATH Z3V FOZ · 2012-04-16
K093546 — SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX FOZ · 2009-12-17
K081953 — SUPERCATH 5 FOZ · 2009-03-12
K052267 — SUPERCATH V FIE · 2006-10-27
K060190 — SUPER SHEATH XL INTRODUCER SHEATH DYB · 2006-04-04
K052557 — SUPER SHEATH INTRODUCER SHEATH DRE · 2006-01-17
K050114 — SUPERCATH Z3V FOZ · 2005-06-09
K864038 — SUPERCATH I.V. CATHETER FOZ · 1986-12-04
K854773 — SUPERCATH A.V. FISTULA FIE · 1986-04-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.