510(k) K202529 ยท LRK Device, Anti-Snoring
ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring
| Applicant | Prosomnus Sleep Technologies, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Nov 20, 2020 |
| Received | Sep 1, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K202529
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.