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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Regulator, Vacuum
510(k) Number K926140
Device Name VACUUM POWER BODY FLUID SUCTION APPARATUS
Applicant
Hill-Rom, Inc.
Hwy. 46
Batesville,  TN 
Applicant Contact FORD WILDER
Correspondent
Hill-Rom, Inc.
Hwy. 46
Batesville,  TN 
Correspondent Contact FORD WILDER
Regulation Number880.6740
Classification Product Code
KDP  
Subsequent Product Code
GCX  
Date Received12/07/1992
Decision Date 07/27/1993
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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