Last synced on 25 January 2026 at 3:41 am

LOGIQ Fortis

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K253366
510(k) Type
Traditional
Applicant
Ge Medical Systems Ultrasound and Primary Care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2026
Days to Decision
99 days
Submission Type
Summary

LOGIQ Fortis

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K253366
510(k) Type
Traditional
Applicant
Ge Medical Systems Ultrasound and Primary Care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/2026
Days to Decision
99 days
Submission Type
Summary