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LOGIQ Totus

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232381
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2023
Days to Decision
121 days
Submission Type
Summary

LOGIQ Totus

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232381
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/7/2023
Days to Decision
121 days
Submission Type
Summary