FDA 510(k), K142160, LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k), K142160, LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM

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510(K) Number: K142160
Device Name: LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM
Manufacturer:
Device Classification Name: System, Imaging, Pulsed Doppler, Ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 08/06/2014
Decision Date: 10/10/2014
Regulation Medical Specialty: Radiology
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