FDA 510(k), K120161, ALPHAPOINT IMAGING SOFTWARE

FDA 510(k), K120161, ALPHAPOINT IMAGING SOFTWARE

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510(K) Number: K120161
Device Name: ALPHAPOINT IMAGING SOFTWARE
Manufacturer: RADLOGICS, INC.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 01/19/2012
Decision Date: 04/13/2012
Regulation Medical Specialty: Radiology

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