FDA 510(k) Applications Submitted by Murata Vios, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K241728 06/14/2024 Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software 2050 Murata Vios, Inc.
K232354 08/07/2023 Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software Murata Vios, Inc.


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