510(k) K223901 ยท LRK Device, Anti-Snoring
ApneaRX Pro
| Applicant | Apnea Sciences Coporation, Aliso Viejo CA, US |
| Decision | Substantially Equivalent, Sep 1, 2023 |
| Received | Dec 28, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K223901
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.