FDA 510(k), K123564, LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k), K123564, LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM

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510(K) Number: K123564
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: 11/20/2012
Decision Date: 12/18/2012
Regulation Medical Specialty: Radiology
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