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LOGIQ P10, LOGIQ P9, LOGIQ P8

Page Type
Cleared 510(K)
510(k) Number
K214039
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2022
Days to Decision
89 days
Submission Type
Summary

LOGIQ P10, LOGIQ P9, LOGIQ P8

Page Type
Cleared 510(K)
510(k) Number
K214039
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2022
Days to Decision
89 days
Submission Type
Summary