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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 K081985
Device Name AW SERVER
Original Applicant
GE MEDICAL SYSTEMS, LLC
3000 n grandview blvd.
w706
waukesha,  WI  53188
Original Contact stephen slavens
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received07/14/2008
Decision Date 09/25/2008
Decision substantially equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
summary summary
Type Traditional
Reviewed by Third Party Yes
Combination Product No
Recalls CDRH Recalls
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