Phenox Limited
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest FDA decision2025-02-28
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K242676 | pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device | POL | 2025-02-28 | View |
| 510(k) | K231539 | pRESET LITE Thrombectomy Device | POL | 2023-10-21 | View |
| 510(k) | K222848 | pRESET Thrombectomy Device | POL | 2023-01-20 | View |
| 510(k) | K191687 | pORTAL Steerable Hydrophilic Guidewire and pORTAL EXT Extension Wire | DQX | 2019-10-09 | View |
No matching devices.
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