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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, non-tilting, powered
510(k) Number K971452
Device Name MULTIX TOP/PRO RADIOGRAPHIC X-RAY TABLE
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
186 WOOD AVE. SOUTH
ISELIN,  NJ  08830
Applicant Contact JEFFREY W KOONTZ
Correspondent
SIEMENS MEDICAL SOLUTIONS USA, INC.
186 WOOD AVE. SOUTH
ISELIN,  NJ  08830
Correspondent Contact JEFFREY W KOONTZ
Regulation Number892.1980
Classification Product Code
IZZ  
Date Received04/21/1997
Decision Date 05/14/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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