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VIVID I AND VIVID Q

Page Type
Cleared 510(K)
510(k) Number
K082374
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/2/2008
Days to Decision
15 days
Submission Type
Summary

VIVID I AND VIVID Q

Page Type
Cleared 510(K)
510(k) Number
K082374
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/2/2008
Days to Decision
15 days
Submission Type
Summary