FDA 510(k) Application Details - K031711

Device Classification Name	Wheelchair, Powered   More FDA Info for this Device
510(K) Number	K031711
Device Name	Wheelchair, Powered
Applicant	AMERICAN BANTEX CORP. 994 NORTH MAIN STREET BOUNTIFUL, UT 84010 US Other 510(k) Applications for this Company
Contact	TRACY S BEST Other 510(k) Applications for this Contact
Regulation Number	890.3860   More FDA Info for this Regulation Number
Classification Product Code	ITI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/02/2003
Decision Date	12/18/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review