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Murata Vios, Inc.

4 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Vios Monitoring System Bedside Monitor Model BSM2050 recall (Z-1292-2025)Murata Vios, Inc.2025-03-06
Vios Monitoring System Bedside Monitor, Model BSM2050, Software Version Numbers 1.54.20 an recall (Z-1169-2025)Murata Vios, Inc.2025-02-12
muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachome recall (Z-1069-2025)Murata Vios, Inc.2025-01-30
muRata Vios Monitoring System Model 2050; bedside cardiac monitor, including cardiotachome recall (Z-0956-2025)Murata Vios, Inc.2025-01-16

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Every clearance here is in the API, with alerts when new ones post.