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MODIFICATION TO GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092079
510(k) Type
Special
Applicant
Ge Medical Systems Israel, Ultrasound, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2009
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092079
510(k) Type
Special
Applicant
Ge Medical Systems Israel, Ultrasound, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2009
Days to Decision
28 days
Submission Type
Summary