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GE LOGIQ 500 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970901
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1997
Days to Decision
286 days
Submission Type
Summary

GE LOGIQ 500 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K970901
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1997
Days to Decision
286 days
Submission Type
Summary