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GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2

Page Type
Cleared 510(K)
510(k) Number
K082185
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2008
Days to Decision
14 days
Submission Type
Summary

GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2

Page Type
Cleared 510(K)
510(k) Number
K082185
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/15/2008
Days to Decision
14 days
Submission Type
Summary