510(k) K213475 ยท LRK Device, Anti-Snoring
Elevo Snoring Intervention Set
| Applicant | Zelegent, Inc., La Jolla CA, US |
| Decision | Substantially Equivalent, Jan 27, 2022 |
| Received | Oct 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213475
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.