Last synced on 25 April 2025 at 11:05 pm

Vivid E80, Vivid E90, Vivid E95

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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