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FDA 510(k) Applications Submitted by GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K082374
08/18/2008
VIVID I AND VIVID Q
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
K092140
07/15/2009
GE VIVID I DIAGNOSTIC ULTRASOUND, GE VIVID Q DIAGNOSTIC ULTRASOUND
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
K092079
07/09/2009
MODIFICATION TO GE VIVID S5 AND S6 DIAGNOSTIC ULTRASOUND
GE MEDICAL SYSTEMS ISRAEL, ULTRASOUND, LTD.
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