510(k) DEN200076 ยท QWE Hyperoxia Monitoring Device Adjunct To Pulse Oximetry
ORi
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Unknown, Oct 12, 2023 |
| Received | Dec 21, 2020 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN200076
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.