510(k) K214096 ยท LRK Device, Anti-Snoring
Respire Clear
| Applicant | Respire Medical, LLC, Brooklyn NY, US |
| Decision | Substantially Equivalent, May 31, 2022 |
| Received | Dec 28, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K214096
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.