510(k) K233618 ยท LEL Device, Sleep Assessment
Oxevision Sleep Device
| Applicant | Oxehealth Limited, Oxford, GB |
| Decision | Substantially Equivalent, Apr 3, 2024 |
| Received | Nov 13, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233618
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.