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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
K181685
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2018
Days to Decision
121 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
K181685
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2018
Days to Decision
121 days
Submission Type
Summary