Medical Device Manufacturer · US , Woodbury , MN

Murata Vios, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Murata Vios, Inc. Cardiovascular ✕
2 devices
1-2 of 2
Cleared Jan 23, 2025
Vios Monitoring System(TM) Model 2050
K241728 · DXN
Cardiovascular · 223d
Cleared Mar 22, 2024
Vios Monitoring System(TM) Model 2050
K232354 · DRT
Cardiovascular · 228d
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