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GE LOGIQ I/E & VIVID E COMPACT DIAGNOSTIC ULTRASOUND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102256
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS CHINA CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
56 days
Submission Type
Summary

GE LOGIQ I/E & VIVID E COMPACT DIAGNOSTIC ULTRASOUND

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102256
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS CHINA CO., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
56 days
Submission Type
Summary