Walk Vascular, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Walk Vascular, LLC - FDA 510(k) Cleared Devices
Recent clearances: JETi AIO Peripheral Thrombectomy System, JETi AIO Peripheral Thrombectomy System, JETi Peripheral Thrombectomy System
9
Total
7
Cleared
0
Denied
Walk Vascular, LLC has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.
Last cleared in 2022. Active since 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Walk Vascular, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Paul Gasser as regulatory consultant.
FDA 510(k) Regulatory Record - Walk Vascular, LLC
9 devices
Cleared
Feb 01, 2022
JETi AIO Peripheral Thrombectomy System
Cardiovascular
84d
Cleared
Nov 17, 2020
JETi AIO Peripheral Thrombectomy System
Cardiovascular
120d
Cleared
Dec 09, 2019
JETi Peripheral Thrombectomy System
Cardiovascular
94d
Cleared
Apr 17, 2019
JETi 88 Peripheral Thrombectomy System
Cardiovascular
131d
Cleared
Oct 24, 2017
ClearLumen II Peripheral Thrombectomy System
Cardiovascular
113d
Cleared
Feb 21, 2017
ClearLumen II Peripheral Thrombectomy System
Cardiovascular
112d
Cleared
Oct 18, 2016
ClearLumen II Thrombectomy System
Cardiovascular
111d
Cleared
Dec 02, 2014
CLEARLUMEN THROMBECTOMY SYSTEM
Cardiovascular
299d
Cleared
Nov 07, 2012
CLEARLUMEN THROMBECTOMY SYSTEM
Cardiovascular
260d