510(k) K233987 · LEL Device, Sleep Assessment
VERABAND
| Applicant | Arbor Medical Innovations, LLC, Saline MI, US |
| Decision | Substantially Equivalent, Jun 17, 2024 |
| Received | Dec 18, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233987
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.