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Vivid E80, Vivid E90, Vivid E95

Page Type
Cleared 510(K)
510(k) Number
K220882
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
119 days
Submission Type
Summary

Vivid E80, Vivid E90, Vivid E95

Page Type
Cleared 510(K)
510(k) Number
K220882
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
119 days
Submission Type
Summary