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FDA 510(k) K082185, GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2, by Ge Medical Systems Ultrasound and Primary Care Dia

FDA 510(k) K082185, GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2, by Ge Medical Systems Ultrasound and Primary Care Dia

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510(K) Number: K082185
Device Name: GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2
Manufacturer: Ge Medical Systems Ultrasound and Primary Care Dia
Device Classification Name: system, imaging, pulsed echo, ultrasonic
Regulation Number: 892.1560
Classification Product Code: IYO
Date Received: 08/01/2008
Decision Date: 08/15/2008
Regulation Medical Specialty: Radiology
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