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Interson USB Ultrasound System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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