FDA 510(k) K103477, PERMOBIL M300 / M400, by Permobil AB

510(K) Number: K103477
Device Name: PERMOBIL M300 / M400
Manufacturer: Permobil AB
Device Classification Name: wheelchair, powered
Regulation Number: 890.3860
Classification Product Code: ITI
Date Received: 11/26/2010
Decision Date: 03/03/2011
Regulation Medical Specialty: Physical Medicine