510(k) K172859 ยท PLC Sleep Appliances With Patient Monitoring
Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder
| Applicant | Prosomnous Sleep Technologies, Pleasanton CA, US |
| Decision | Substantially Equivalent, Nov 22, 2017 |
| Received | Sep 20, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172859
No recall in the FDA data names this 510(k).
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