FDA 510(k), K173420, Radiomics App v1.0

FDA 510(k), K173420, Radiomics App v1.0

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510(K) Number: K173420
Device Name: Radiomics App v1.0
Manufacturer: Microsoft Corp.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 11/01/2017
Decision Date: 12/27/2017
Regulation Medical Specialty: Radiology

Total pages: 435
Fully redacted pages: 362
Content pages: 73

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