510(k) K230532 ยท LQZ Device, Jaw Repositioning
RADx Intraoral Appliance for Snoring and Sleep Apnea
| Applicant | Achaemenid, LLC, Stratford CT, US |
| Decision | Substantially Equivalent, Jul 12, 2023 |
| Received | Feb 27, 2023 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K230532
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.