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V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K223387
510(k) Type
Traditional
Applicant
Samsung Medison Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/13/2023
Days to Decision
98 days
Submission Type
Summary

V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K223387
510(k) Type
Traditional
Applicant
Samsung Medison Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
2/13/2023
Days to Decision
98 days
Submission Type
Summary