Terumo Cardiovascular Systems Corporation - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Terumo Cardiovascular Systems Corporation has 29 FDA 510(k) cleared cardiovascular devices. Based in Elkton, US.
Latest FDA clearance: Apr 2024. Active since 2002.
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 Cardiovascular Systems...
29 devices
Cleared
Apr 25, 2024
CDI OneView Monitoring System
Cardiovascular
125d
Cleared
Apr 18, 2023
Terumo Advanced Perfusion System 1
Cardiovascular
292d
Cleared
Nov 18, 2021
Capiox iCP Centrifugal Pump
Cardiovascular
672d
Cleared
Nov 02, 2018
CDI Blood Parameter Monitoring System 550
Cardiovascular
88d
Cleared
Jun 22, 2018
Terumo Capiox NX19 Oxygenator with Reservoir (east Orientation), Terumo...
Cardiovascular
72d
Cleared
Mar 29, 2018
Terumo Capiox NX19 Oxygenator with Reservoir (east orientation ), Terumo...
Cardiovascular
262d
Cleared
Aug 17, 2017
Advanced Perfusion System 1
Cardiovascular
24d
Cleared
Jun 07, 2017
Advanced Perfusion System 1
Cardiovascular
173d
Cleared
Nov 17, 2016
Small (4) Roller Pump for the Terumo Advanced Perfusion System 1, Large (6)...
Cardiovascular
37d
Cleared
Apr 21, 2016
VirtuoSaph Plus Endoscopic Vessel Harvesting System
General & Plastic Surgery
84d
Cleared
Dec 16, 2015
Advanced Perfusion System 1
Cardiovascular
23d
Cleared
Dec 03, 2015
Capiox RX Hollow Fiber Oxygenator with/without Hardshell Reservoir
Cardiovascular
28d