FDA 510(k) Applications Submitted by GE MEDICAL SYSTEM ISRAEL LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K121062 04/06/2012 VIVID I DIAGNOSTIC ULTRASOUND SYSTEM, VIVID Q DIAGNOSTIC ULTRASOUND SYSTEM GE MEDICAL SYSTEM ISRAEL LTD.
K121063 04/06/2012 VIVID S5 DIAGNOSTIC ULTRASOUND SYSTEM, VIVID S6 DIAGNOSTIC ULTRASOUND SYSTEM GE MEDICAL SYSTEM ISRAEL LTD.
K102388 08/23/2010 VIVID I DIAGNOSTIC ULTRASOUND SYSTEM GE MEDICAL SYSTEM ISRAEL LTD.
K102393 08/23/2010 VIVID S5 DIAGNOSTIC ULTRASOUND SYSTEM; VIVID S6 DIAGNOSTICULTRASOUND SYSTEM GE MEDICAL SYSTEM ISRAEL LTD.


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