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LOGIQ P10, LOGIQ P9, LOGIQ P8

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203114
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2021
Days to Decision
85 days
Submission Type
Summary

LOGIQ P10, LOGIQ P9, LOGIQ P8

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203114
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/8/2021
Days to Decision
85 days
Submission Type
Summary