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LOGIQ E10s, LOGIQ Fortis

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231989
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostic,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2023
Days to Decision
125 days
Submission Type
Summary

LOGIQ E10s, LOGIQ Fortis

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231989
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostic,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/7/2023
Days to Decision
125 days
Submission Type
Summary