510(k) K233754 ยท LQZ Device, Jaw Repositioning
AIO Breathe
| Applicant | Aiomega, LLC, Tyler TX, US |
| Decision | Substantially Equivalent, Feb 23, 2024 |
| Received | Nov 22, 2023 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K233754
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.