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V8/XV8/XH8, V7/XV7/XH7, V6/XV6/XH6 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240631
510(k) Type
Traditional
Applicant
Samsung Medison Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/21/2024
Days to Decision
107 days
Submission Type
Summary

V8/XV8/XH8, V7/XV7/XH7, V6/XV6/XH6 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240631
510(k) Type
Traditional
Applicant
Samsung Medison Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
6/21/2024
Days to Decision
107 days
Submission Type
Summary