ClearanceBrief
Company ยท US

Walk Vascular, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2022. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QEZAspiration Thrombectomy Catheter9

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 1, 2022K213565JETi AIO Peripheral Thrombectomy System
Walk Vascular, LLC
QEZ
Nov 17, 2020K201998JETi AIO Peripheral Thrombectomy System
Walk Vascular, LLC
QEZ
Dec 9, 2019K192439JETi Peripheral Thrombectomy System
Walk Vascular, LLC
QEZ
Apr 17, 2019K183403JETi 88 Peripheral Thrombectomy System
Walk Vascular, LLC
QEZ
Oct 24, 2017K172000ClearLumen II Peripheral Thrombectomy System
Walk Vascular, LLC
QEZ
Feb 21, 2017K163051ClearLumen II Peripheral Thrombectomy System
Walk Vascular, LLC
QEZ
Oct 18, 2016K161786ClearLumen II Thrombectomy System
Walk Vascular, LLC
QEZ
Dec 2, 2014K140296CLEARLUMEN THROMBECTOMY SYSTEM
Walk Vascular, LLC
QEZ
Nov 7, 2012K120508CLEARLUMEN THROMBECTOMY SYSTEM
Walk Vascular, LLC
QEZ

Latest recalls

DateFirm and productCodeLinked 510(k)
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