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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name table, radiographic, tilting
510(k) Number K945842
Device Name MOBILIX MOBILE X-RAY TABLE
Original Applicant
GE MEDICAL SYSTEMS
po box 414
milwaukee,  WI  53201
Original Contact larry a kroger
Regulation Number892.1980
Classification Product Code
IXR  
Date Received11/30/1994
Decision Date 01/18/1995
Decision substantially equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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