K241728
- 510(k) number
- K241728
- Device name
- Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050
- Applicant
- Murata Vios, Inc. MN · US
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2025-01-23
- Date received
- 2024-06-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K241728.pdf
Official FDA record: K241728
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.