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Murata Vios, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest FDA decision2025-01-23
TypeNumberDevice NameCodeDateActions
510(k) K241728 Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050DXN2025-01-23 View
510(k) K232354 Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server SoftwareDRT2024-03-22 View
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