FDA 510(k), K173619, Mimics inPrint

FDA 510(k), K173619, Mimics inPrint

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510(K) Number: K173619
Device Name: Mimics inPrint
Manufacturer: Materialise NV
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 11/22/2017
Decision Date: 03/21/2018
Regulation Medical Specialty: Radiology

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