510(k) K233497 ยท PLC Sleep Appliances With Patient Monitoring
Rest Assure System
| Applicant | Somnomed, Inc., Plano TX, US |
| Decision | Substantially Equivalent, Oct 3, 2024 |
| Received | Oct 31, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233497
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.