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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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