Prosomnus Sleep Technologies
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K252765 | ProSomnus RPMO2 OSA Device (RPMO2 OSA) | PLC | 2026-04-06 | View |
| 510(k) | K221889 | ProSomnus EVO [PH] Sleep and Snore Device, ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring | LRK | 2022-10-06 | View |
No matching devices.
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