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GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091374
510(k) Type
Traditional
Applicant
Ge Medical Systems China Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/26/2009
Days to Decision
15 days
Submission Type
Summary

GE LOGIQ I/E & VIVID E COMPACT ULTRASOUND

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091374
510(k) Type
Traditional
Applicant
Ge Medical Systems China Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/26/2009
Days to Decision
15 days
Submission Type
Summary