510(k) K203477 ยท LRK Device, Anti-Snoring
Classic
| Applicant | Orthoapnea S.L., Malaga, ES |
| Decision | Substantially Equivalent, Feb 25, 2021 |
| Received | Nov 27, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203477
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.