FDA 510(k), K021075, MECHANICAL DAILY USE WHEELCHAIR

FDA 510(k), K021075, MECHANICAL DAILY USE WHEELCHAIR

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510(K) Number: K021075
Device Name: MECHANICAL DAILY USE WHEELCHAIR
Manufacturer: FIRST WORLD SERVICES, INC.
Device Classification Name: wheelchair, mechanical
Regulation Number: 890.3850
Classification Product Code: IOR
Date Received: 04/02/2002
Decision Date: 07/12/2002
Regulation Medical Specialty: Physical Medicine

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