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Interson USB Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K233734
510(k) Type
Special
Applicant
Interson Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2023
Days to Decision
30 days
Submission Type
Summary

Interson USB Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K233734
510(k) Type
Special
Applicant
Interson Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2023
Days to Decision
30 days
Submission Type
Summary