510(k) K250482 ยท LRK Device, Anti-Snoring
Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue
| Applicant | Fissiontech, LLC, New York NY, US |
| Decision | Substantially Equivalent, May 8, 2025 |
| Received | Feb 19, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250482
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.