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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stretcher, Wheeled
510(k) Number K874332
Device Name MRI STRETCHER
Applicant
Atomic Products Corp.
P.O. Drawer R
Shirley,  NY  11967
Applicant Contact JAMES REISS
Correspondent
Atomic Products Corp.
P.O. Drawer R
Shirley,  NY  11967
Correspondent Contact JAMES REISS
Regulation Number880.6910
Classification Product Code
FPO  
Date Received10/22/1987
Decision Date 01/05/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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