FDA 510(k), K151115, MR Core Software

FDA 510(k), K151115, MR Core Software

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510(K) Number: K151115
Device Name: MR Core Software
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 04/27/2015
Decision Date: 06/03/2015
Regulation Medical Specialty: Radiology
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