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GE LOGIQ700 DIAGNOSTIC ULTRASOUND SYSTEM WITH B-FLOW

Page Type
Cleared 510(K)
510(k) Number
K990226
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1999
Days to Decision
15 days
Submission Type
Summary

GE LOGIQ700 DIAGNOSTIC ULTRASOUND SYSTEM WITH B-FLOW

Page Type
Cleared 510(K)
510(k) Number
K990226
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/9/1999
Days to Decision
15 days
Submission Type
Summary