Volcano Corporation - FDA 510(k) Cleared Devices
55
Total
55
Cleared
0
Denied
FDA 510(k) cleared devices by Volcano Corporation Cardiovascular ✕
26 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
Feb 11, 2019
IntraSight
Cardiovascular
26d
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
Cleared
Dec 31, 2015
Visions PV .035 Digital IVUS Catheter
Cardiovascular
66d
Cleared
Dec 03, 2015
CORE FM System, Patient Interface Module (OPIM), Hemodynamic Converter Box
Cardiovascular
84d
Cleared
Nov 19, 2015
Visions PV.014P RX Digital IVUS Catheter
Cardiovascular
51d
Cleared
Sep 04, 2015
Volcano Visions PV .018 Digital IVUS Catheter
Cardiovascular
196d
Cleared
Aug 26, 2015
EAGLE EYE PLATINUM CATHETER, EAGLE EYE PLATINUM SHORT TIP CATHETER, VISIONS...
Cardiovascular
245d