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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 K893129
Device Name CXC FFT-1 NON-TILT STAT RADIO XRAY TAB 4 WA FL TAB
Applicant
Continental X-Ray Corp.
Post Office Box 5571
Chicago,  IL  60680
Applicant Contact ROBERT D WALKER
Correspondent
Continental X-Ray Corp.
Post Office Box 5571
Chicago,  IL  60680
Correspondent Contact ROBERT D WALKER
Regulation Number892.1980
Classification Product Code
IZZ  
Date Received04/25/1989
Decision Date 06/01/1989
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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