510(k) K210636 ยท LRK Device, Anti-Snoring
Morpheus
| Applicant | S4S UK , Ltd., Sheffield, GB |
| Decision | Substantially Equivalent, Feb 15, 2022 |
| Received | Feb 19, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210636
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.