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LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3

Page Type
Cleared 510(K)
510(k) Number
K161224
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2016
Days to Decision
98 days
Submission Type
Summary

LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3

Page Type
Cleared 510(K)
510(k) Number
K161224
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound & Primary Care Diagnostics LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2016
Days to Decision
98 days
Submission Type
Summary