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Vasoinnovations, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K203803VASOBand Vascular Compression DeviceJanuary 26, 2021
K190318VASOBand Vascular Compression DeviceMarch 14, 2019