Walk Vascular, LLC
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K213565 | JETi AIO Peripheral Thrombectomy System | QEZ | 2022-02-01 | View |
| 510(k) | K201998 | JETi AIO Peripheral Thrombectomy System | QEZ | 2020-11-17 | View |
| 510(k) | K192439 | JETi Peripheral Thrombectomy System | QEZ | 2019-12-09 | View |
| 510(k) | K183403 | JETi 88 Peripheral Thrombectomy System | QEZ | 2019-04-17 | View |
| 510(k) | K172000 | ClearLumen II Peripheral Thrombectomy System | QEZ | 2017-10-24 | View |
| 510(k) | K163051 | ClearLumen II Peripheral Thrombectomy System | QEZ | 2017-02-21 | View |
| 510(k) | K161786 | ClearLumen II Thrombectomy System | QEZ | 2016-10-18 | View |
| 510(k) | K120508 | CLEARLUMEN THROMBECTOMY SYSTEM | QEZ | 2012-11-07 | View |
No matching devices.
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