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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, tomographic
510(k) Number K925302
Device Name PHILIPS INTEGRIS H/HM SYSTEM
Applicant
PHILIPS MEDICAL SYSTEMS, INC.
VEENPLUIS 4-6
P.O. BOX 10000
5680 DA BEST,  NL
Applicant Contact WILLIAM G MCMAHON
Correspondent
PHILIPS MEDICAL SYSTEMS, INC.
VEENPLUIS 4-6
P.O. BOX 10000
5680 DA BEST,  NL
Correspondent Contact WILLIAM G MCMAHON
Regulation Number892.1740
Classification Product Code
IZF  
Date Received10/21/1992
Decision Date 12/17/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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