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Intravu, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K243020MIDASVuDecember 2, 2024
K181982MIDAScope and Introducer Kit, and MIDASystemAugust 21, 2018