FDA 510(k) Application Details - K062483

Device Classification Name	Wheelchair, Powered   More FDA Info for this Device
510(K) Number	K062483
Device Name	Wheelchair, Powered
Applicant	LINE IND.(SHANGHAI) CO., LTD. 55 Northern Blvd. Suite 200 Great Neck, NY 11021 US Other 510(k) Applications for this Company
Contact	SID MATHUR 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	08/25/2006
Decision Date	09/08/2006
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	Y
Expedited Review