Last synced on 14 November 2025 at 11:06 pm

V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System; V5 Diagnostic Ultrasound System; cV5 Diagnostic Ultrasound System; V4 Diagnostic Ultrasound System; cV4 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K250999
510(k) Type
Traditional
Applicant
Samsung Medison Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/18/2025
Days to Decision
108 days
Submission Type
Summary

V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System; V5 Diagnostic Ultrasound System; cV5 Diagnostic Ultrasound System; V4 Diagnostic Ultrasound System; cV4 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K250999
510(k) Type
Traditional
Applicant
Samsung Medison Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/18/2025
Days to Decision
108 days
Submission Type
Summary