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LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160277
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2016
Days to Decision
52 days
Submission Type
Summary

LOGIQ F8 Expert, LOGIQ F8, LOGIQ F6

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160277
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/2016
Days to Decision
52 days
Submission Type
Summary