510(k) K250757 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Radius VSM and Accessories
| Applicant | Masimo Corporation, Irvine CA, US |
| Decision | Substantially Equivalent, May 29, 2025 |
| Received | Mar 12, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K250757
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.