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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 K103785
FOIA Releasable 510(k) K103785
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  
Date Received12/27/2010
Decision Date 02/04/2011
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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