FDA 510(k) K112930, MOBILE MIM, by Mim Software, Inc.

510(K) Number: K112930
Device Name: MOBILE MIM
Manufacturer: Mim Software, Inc.
Device Classification Name: system, image processing, radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 10/03/2011
Decision Date: 12/02/2011
Regulation Medical Specialty: Radiology