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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Bed, Ac-Powered Adjustable Hospital
510(k) Number K890845
Device Name PREMISE SERIES BED
Applicant
Batesville American Mfg. Co.
P.O. Box 838
Batesville,  MS  38606
Applicant Contact DAVID SMITH
Correspondent
Batesville American Mfg. Co.
P.O. Box 838
Batesville,  MS  38606
Correspondent Contact DAVID SMITH
Regulation Number880.5100
Classification Product Code
FNL  
Date Received02/21/1989
Decision Date 06/15/1989
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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