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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