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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name system, x-ray, stationary
510(k) Number K001201
Device Name MULTIX COMPACT K AND MULTIX L RADIOGRAPHIC X-RAY SYSTEMS
Original Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
186 wood avenue south
iselin,  NJ  08830
Original Contact malgorzata stanek
Regulation Number892.1680
Classification Product Code
KPR  
Date Received04/13/2000
Decision Date 06/01/2000
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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