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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 K853593
Device Name VESSA TRAVVLA
Applicant
Vessa , Ltd.
Paper Mill Ln.
Alton Hampshire
Gu34 2p4 England,  GB
Applicant Contact IAN D JONES
Correspondent
Vessa , Ltd.
Paper Mill Ln.
Alton Hampshire
Gu34 2p4 England,  GB
Correspondent Contact IAN D JONES
Regulation Number890.3860
Classification Product Code
ITI  
Date Received08/27/1985
Decision Date 09/24/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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