Togo Medikit Co., Ltd. - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Togo Medikit Co., Ltd. has 17 FDA 510(k) cleared medical devices. Based in Chiyoda-Ku Tokyo101 Japan, JP.
Latest FDA clearance: Sep 2024. Active since 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Togo Medikit Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mic International Corp. as regulatory consultant.
17 devices
Cleared
Sep 17, 2024
Super Sheath Introducer Sheath S-3N5/1005 S-3N7/1006 S-3W5/1007 S-3W7/1008
Cardiovascular
138d
Cleared
Mar 19, 2020
Super Sheath
Cardiovascular
30d
Cleared
Sep 20, 2019
Supercath 5
General Hospital
261d
Cleared
Mar 23, 2018
SUPERCATH 5 (26G)
General Hospital
217d
Cleared
Aug 12, 2016
SUPERCATH 6
General Hospital
164d
Cleared
Jan 15, 2015
SUPER SHEATH
Cardiovascular
265d
Cleared
May 12, 2014
SUPERCATH5
General Hospital
83d
Cleared
Sep 27, 2012
SUPER SHEATH INTRODUCER SHEATH AND SUPER SHEATH INTRODUCER SHEATH SETS
Cardiovascular
129d
Cleared
Apr 16, 2012
SUPERCATH Z3V
General Hospital
251d
Cleared
Dec 17, 2009
SUPERCATH 5 MODEL SP120-XX-XX, SP125-XX-XX
General Hospital
30d
Cleared
Mar 12, 2009
SUPERCATH 5
General Hospital
246d
Cleared
Oct 27, 2006
SUPERCATH V
Gastroenterology & Urology
434d