FDA 510(k), K113663, SONIXTABLET ULTRASOUND SCANNER

FDA 510(k), K113663, SONIXTABLET ULTRASOUND SCANNER

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510(K) Number: K113663
Device Name: SONIXTABLET ULTRASOUND SCANNER
Manufacturer:
Device Classification Name: System, Imaging, Pulsed Doppler, Ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 12/13/2011
Decision Date: 01/25/2012
Regulation Medical Specialty: Radiology
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