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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Scanner, Rectilinear, Nuclear
510(k) Number K895799
Device Name RECTILINEAR SCANNER MODEL #187-270
Applicant
Atomic Products Corp.
P.O. Drawer R
Shirley,  NY  11967
Applicant Contact CLYDE SCHLEIN
Correspondent
Atomic Products Corp.
P.O. Drawer R
Shirley,  NY  11967
Correspondent Contact CLYDE SCHLEIN
Regulation Number892.1300
Classification Product Code
IYW  
Date Received09/28/1989
Decision Date 02/01/1990
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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