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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Obstetrical, Ac-Powered (And Accessories)
510(k) Number K914309
Device Name THE GENESIS BED FROM HILL-ROM, MODEL 355 SERIES
Applicant
HILL-ROM, INC.
HIGHWAY 46
BATESVILLE,  TN 
Applicant Contact FORD WILDER
Correspondent
HILL-ROM, INC.
HIGHWAY 46
BATESVILLE,  TN 
Correspondent Contact FORD WILDER
Regulation Number884.4900
Classification Product Code
HDD  
Date Received09/25/1991
Decision Date 04/20/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Obstetrics/Gynecology
510k Review Panel Obstetrics/Gynecology
Type Traditional
Reviewed by Third Party No
Combination Product No
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