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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name wheelchair, powered
510(k) Number K010859
Device Name THE LIBERATOR WHEELCHAIR
Applicant
LIBERATOR WHEELCHAIRS, INC.
3402-B N. BEACH ST.
HALTON CITY,  TX  76111
Applicant Contact RICARDO KAUFMANN
Correspondent
LIBERATOR WHEELCHAIRS, INC.
3402-B N. BEACH ST.
HALTON CITY,  TX  76111
Correspondent Contact RICARDO KAUFMANN
Regulation Number890.3860
Classification Product Code
ITI  
Date Received03/22/2001
Decision Date 04/05/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Special
Reviewed by Third Party No
Combination Product No
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