# Walk Vascular, LLC

- Location (FDA's records): Irvine, CA
- FDA decisions: 9 (2012–2022): 9 510(k) clearances
- Product codes: QEZ (9)
- 510(k) review time since 2016: median 113 days, against 112 for FDA's reviews in the same codes and years (0 of 5 faster)
- Predicates its devices cite: 12 (6 its own); citations of its devices by later devices: 7 (6 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Vascular: 3 (https://510kreport.com/company/medtronic-vascular)
- Kerberos Proximal Solutions, Inc.: 1 (https://510kreport.com/company/kerberos-proximal-solutions)
- Possis Medical, Inc.: 1 (https://510kreport.com/company/possis-medical)
- Ev3, Inc.: 1 (https://510kreport.com/company/ev3)

## Firms that cite its devices most
- Abbott Medical: 1 (https://510kreport.com/company/abbott-medical)

## Its most-cited devices
- K183403: JETi 88 Peripheral Thrombectomy System (2019), cited by 2
- K120508: Clearlumen Thrombectomy System (2012), cited by 1
- K213565: JETi AIO Peripheral Thrombectomy System (2022), cited by 1
- K161786: ClearLumen II Thrombectomy System (2016), cited by 1
- K201998: JETi AIO Peripheral Thrombectomy System (2020), cited by 1
- K140296: Clearlumen Thrombectomy System (2014), cited by 1

## Recent decisions
- K213565: JETi AIO Peripheral Thrombectomy System (Feb 1, 2022)
- K201998: JETi AIO Peripheral Thrombectomy System (Nov 17, 2020)
- K192439: JETi Peripheral Thrombectomy System (Dec 9, 2019)
- K183403: JETi 88 Peripheral Thrombectomy System (Apr 17, 2019)
- K172000: ClearLumen II Peripheral Thrombectomy System (Oct 24, 2017)
- K163051: ClearLumen II Peripheral Thrombectomy System (Feb 21, 2017)
- K161786: ClearLumen II Thrombectomy System (Oct 18, 2016)
- K140296: Clearlumen Thrombectomy System (Dec 2, 2014)

Source page: https://510kreport.com/company/walk-vascular