Volcano Corporation - FDA 510(k) Cleared Devices
55
Total
55
Cleared
0
Denied
Volcano Corporation has 55 FDA 510(k) cleared medical devices. Based in Rancho Cordova,, US.
Last cleared in 2021. Active since 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Volcano Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Volcano Corporation
55 devices
Cleared
Apr 15, 2021
Verrata PLUS Pressure Guide Wire
Cardiovascular
77d
Cleared
Jan 19, 2021
IntraSight Mobile
Cardiovascular
29d
Cleared
Sep 28, 2020
OmniWire Pressure Guide Wire, 185 cm Straight Tip, OmniWire Pressure Guide...
Cardiovascular
26d
Cleared
Mar 26, 2020
OmniWire Pressure Guide Wire, 185 cm Straight Tip, OmniWire Pressure Guide...
Cardiovascular
168d
Cleared
Apr 12, 2019
SyncVision System
Radiology
32d
Cleared
Feb 11, 2019
IntraSight
Cardiovascular
26d
Cleared
Apr 11, 2018
s5 Intravascular Ultrasound Imaging and Pressure Systems, s5i Intravascular...
Radiology
112d
Cleared
Oct 25, 2017
CORE M2 Vascular System, CORE M2 Software v4.2 Upgrade Kit, CORE M2 Software...
Radiology
72d
Cleared
Oct 05, 2017
SyncVision System
Radiology
38d
Cleared
Apr 06, 2017
CORE M2 Vascular System
Radiology
57d
Cleared
Oct 26, 2016
REFINITY Rotational IVUS Catheter, REFINITY Rotational IVUS Catheter, Short Tip
Cardiovascular
239d
Cleared
Sep 20, 2016
Verrata PLUS Pressure Guide Wire, 185 cm Straight Tip, Verrata PLUS Pressure...
Cardiovascular
71d
Looking for a specific device from Volcano Corporation? Search by device name or K-number.
Search all Volcano Corporation devices