Terumo Medical Corporation - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Terumo Medical Corporation has 14 FDA 510(k) cleared cardiovascular devices. Based in Elkton, US.
Last cleared in 2023. Active since 2011.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Terumo Medical Corporation
14 devices
Cleared
Jul 27, 2023
R2P Navicross
Cardiovascular
106d
Cleared
Dec 20, 2021
TR BAND Radial Compression Device
Cardiovascular
45d
Cleared
Jan 06, 2020
R2P Destination Slender Guiding Sheath
Cardiovascular
55d
Cleared
Aug 03, 2018
Glidesheath Slender Tibial Pedal Kit
Cardiovascular
85d
Cleared
May 08, 2018
Glidesheath Slender
Cardiovascular
141d
Cleared
Nov 21, 2017
Destination Carotid Guiding Sheath, Destination Peripheral Guiding Sheath,...
Cardiovascular
55d
Cleared
Oct 05, 2017
R2P Destination Slender Guiding Sheath
Cardiovascular
136d
Cleared
Dec 01, 2015
Glidesheath
Cardiovascular
119d
Cleared
Nov 10, 2015
TR BAND Radial Compression Device
Cardiovascular
68d
Cleared
Sep 17, 2015
Radifocus Glidewire Endoscopic Wire
Gastroenterology & Urology
108d
Cleared
Nov 21, 2014
GLIDESHEATH SLENDER
Cardiovascular
105d
Cleared
Mar 01, 2013
RADIFOCUS GLIDEWIRE ADVANTAGE, RADIFOCUS GLIDEWIRE ADVANTAGE
Cardiovascular
189d