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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name system, image processing, radiological
510(k) Number K112930
FOIA Releasable 510(k) K112930
Device Name MOBILE MIM
Applicant
MIM SOFTWARE INC.
25200 CHAGRIN BLVD.
SUITE 200
cleveland,  OH  44122
Applicant Contact lynn hanigan
Correspondent
MIM SOFTWARE INC.
25200 CHAGRIN BLVD.
SUITE 200
cleveland,  OH  44122
Correspondent Contact lynn hanigan
Regulation Number892.2050
Classification Product Code
LLZ  
Subsequent Product Code
MUJ  
Date Received10/03/2011
Decision Date 12/02/2011
Decision substantially equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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