FDA 510(k), K110943, LOGIQ E9

FDA 510(k), K110943, LOGIQ E9

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510(K) Number: K110943
Device Name: LOGIQ E9
Manufacturer: GE HEALTHCARE
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 04/04/2011
Decision Date: 07/22/2011
Regulation Medical Specialty: Radiology
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