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GE LOGIQ E9 BT2010 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 5205000-3, 5205000-4

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092271
510(k) Type
Traditional
Applicant
GE HEALTHCARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2009
Days to Decision
112 days
Submission Type
Summary

GE LOGIQ E9 BT2010 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 5205000-3, 5205000-4

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092271
510(k) Type
Traditional
Applicant
GE HEALTHCARE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2009
Days to Decision
112 days
Submission Type
Summary