FDA 510(k) Application Details - K024175

Device Classification Name	Wheelchair, Powered   More FDA Info for this Device
510(K) Number	K024175
Device Name	Wheelchair, Powered
Applicant	SUNPEX TECHNOLOGY CO., LTD. 914 WEST PATAPSCO AVE. BALTIMORE, MD 21230 US Other 510(k) Applications for this Company
Contact	LEONARD FRIER 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	12/18/2002
Decision Date	05/01/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review