510(k) K233850 ยท LRK Device, Anti-Snoring
Difiney Anti Snoring Device
| Applicant | Fissiontech, LLC, New York NY, US |
| Decision | Substantially Equivalent, Apr 18, 2024 |
| Received | Dec 5, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233850
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.