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MODIFICATION TO GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND

Page Type
Cleared 510(K)
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)
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