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Interson Corporation

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K233734Interson USB Ultrasound SystemDecember 22, 2023
K163443Interson USB Ultrasound SystemApril 13, 2017