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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name system, tomography, computed, emission
510(k) Number K923309
Device Name ARGUS PET SYSTEM
Applicant
GE MEDICAL SYSTEMS
3000 N GRANDVIEW BLVD.
W-709
WAUKESHA,  WI  53188
Applicant Contact LARRY A KROGER
Correspondent
GE MEDICAL SYSTEMS
3000 N GRANDVIEW BLVD.
W-709
WAUKESHA,  WI  53188
Correspondent Contact LARRY A KROGER
Regulation Number892.1200
Classification Product Code
KPS  
Date Received07/07/1992
Decision Date 09/29/1992
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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