FDA 510(k) Applications Submitted by ProSomnus Sleep Technologies
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221889 | 06/29/2022 | ProSomnus EVO [PH] Sleep and Snore Device, ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring | ProSomnus Sleep Technologies |
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