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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 K902610
Device Name GENERAL ELECTRIC AMX 3
Applicant
Pro-Tronics, Inc.
652 Pond Dr.
Wood Dale,  IL  60191
Applicant Contact CURT BORK
Correspondent
Pro-Tronics, Inc.
652 Pond Dr.
Wood Dale,  IL  60191
Correspondent Contact CURT BORK
Regulation Number892.1720
Classification Product Code
IZL  
Date Received06/12/1990
Decision Date 07/02/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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