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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Manual
510(k) Number K792298
Device Name THE VERSA-BED
Applicant
FIRST & TEN, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
FIRST & TEN, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number880.5120
Classification Product Code
FNJ  
Date Received11/13/1979
Decision Date 12/20/1979
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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