• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K110943, LOGIQ E9, by GE Healthcare

FDA 510(k) K110943, LOGIQ E9, by GE Healthcare

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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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