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Venturemed Group, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K202187FLEX Vessel Prep SystemSeptember 11, 2020
K152789FLEX SCORING CATHETERMay 25, 2016