Xtreem Pulse, LLC
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K262861 | PureLift Pro Max | NFO | 2026-09-11 | View |
| 510(k) | K243587 | PureLift GLOW | NFO | 2025-03-06 | View |
| 510(k) | K221443 | PureLift Pro Plus | NFO | 2022-10-21 | View |
| 510(k) | K190269 | PureLift | NFO | 2019-08-28 | View |
| 510(k) | K173483 | Pure Flow External Counter-Pulsation Device | DRN | 2018-05-30 | View |
No matching devices.
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