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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
K170823
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2017
Days to Decision
84 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
K170823
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2017
Days to Decision
84 days
Submission Type
Summary