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Sonavex, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243479EchoGuide (Version 1)April 23, 2025
K190039EchoSure Diagnostic Ultrasound SystemMarch 8, 2019
K180621EchoMark, EchoMark LPJune 6, 2018