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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 K123375
Device Name SYNGO.VIA
Applicant
SIEMENS AG
HENKESTRASSE 127
ERLANGEN, BAVARIA,  DE 91052
Applicant Contact SABINE SCHROEDEL
Correspondent
TUV SUD AMERICA INC.
1775 OLD HIGHWAY 8 NW
NEW BRIGHTON,  MN  55112 -1891
Regulation Number892.2050
Classification Product Code
LLZ  
Date Received11/01/2012
Decision Date 11/20/2012
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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