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Vivid T8, Vivid T9

Page Type
Cleared 510(K)
510(k) Number
K221147
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2022
Days to Decision
89 days
Submission Type
Summary

Vivid T8, Vivid T9

Page Type
Cleared 510(K)
510(k) Number
K221147
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2022
Days to Decision
89 days
Submission Type
Summary