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Vivid S60N, Vivid S70N

Page Type
Cleared 510(K)
510(k) Number
K220619
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
134 days
Submission Type
Summary

Vivid S60N, Vivid S70N

Page Type
Cleared 510(K)
510(k) Number
K220619
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2022
Days to Decision
134 days
Submission Type
Summary