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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lift, Patient, Ac-Powered
510(k) Number K903723
Device Name BARRIER FREE CEILING LIFT, MDLS HRS-1/2F,1/4F,1/6F
Applicant
Barrier Free Lifts, Inc.
10511 Pineview Rd.
Manassas,  VA  22111
Applicant Contact THEODORE M HENSLEY
Correspondent
Barrier Free Lifts, Inc.
10511 Pineview Rd.
Manassas,  VA  22111
Correspondent Contact THEODORE M HENSLEY
Regulation Number880.5500
Classification Product Code
FNG  
Date Received08/16/1990
Decision Date 09/24/1990
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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