FDA 510(k), K103785, MOBILE MIM

FDA 510(k), K103785, MOBILE MIM

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510(K) Number: K103785
Device Name: MOBILE MIM
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 12/27/2010
Decision Date: 02/04/2011
Regulation Medical Specialty: Radiology
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