510(k) K241728 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050
| Applicant | Murata Vios, Inc., Woodbury MN, US |
| Decision | Substantially Equivalent, Jan 23, 2025 |
| Received | Jun 14, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241728
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.