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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 K973039
Device Name LEGACY/LEGACY-D TABLE
Original Applicant
GE MEDICAL SYSTEMS
p.o. box 414
milwaukee,  WI  53201
Original Contact larry a kroger
Regulation Number892.1980
Classification Product Code
IXR  
Date Received08/14/1997
Decision Date 10/16/1997
Decision substantially equivalent (SE)
Classification Advisory Committee Radiology
Review Advisory Committee Radiology
summary summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
Recalls CDRH Recalls
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