FDA 510(k) Applications Submitted by Prosomnous Sleep Technologies
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K172859 | 09/20/2017 | Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder | Prosomnous Sleep Technologies |
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