510(k) K232354

Device
Vios Monitoring System(TM) Model 2050; Vios Central Station Monitor/Vios Central Server Software
Applicant
Murata Vios, Inc.
510(k) number
K232354
Product code
DRT
Decision
Substantially Equivalent (SESE)
Decision date
2024-03-22
Date received
2023-08-07
Regulation
870.2300
Classification name
Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Amit Patel
Address
700 Commerce Dr., #190 Woodbury MN US 55125 55125

FDA Registration Numbers

Source Documents

510(k) summary PDF

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