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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Changer, Radiographic Film/Cassette
510(k) Number K924423
Device Name MWX-7440 HIGH SPEED BUCKY
Applicant
Midwest X-Ray Equipment Co.
701 W. Illinios Ave.
Aurora,  IL  60506
Applicant Contact ROBERT BROWN
Correspondent
Midwest X-Ray Equipment Co.
701 W. Illinios Ave.
Aurora,  IL  60506
Correspondent Contact ROBERT BROWN
Regulation Number892.1860
Classification Product Code
KPX  
Date Received09/01/1992
Decision Date 01/15/1993
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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