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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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