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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, mobile
510(k) Number K833226
Device Name PMX MOBILE X-RAY SYSTEM
Original Applicant
PHILIPS MEDICAL SYSTEMS, INC.
Regulation Number892.1720
Classification Product Code
IZL  
Date Received08/18/1983
Decision Date 10/28/1983
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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