FDA 510(k) Application Details - K961743

Device Classification Name	Wheelchair, Mechanical   More FDA Info for this Device
510(K) Number	K961743
Device Name	Wheelchair, Mechanical
Applicant	PDG PRODUCT DESIGN GROUP, INC. 9165 SHAUGHNESSY ST., VANCOUVER,BRITISH COLUMBIA V6P 6R9 CA Other 510(k) Applications for this Company
Contact	PHIL MUNDY Other 510(k) Applications for this Contact
Regulation Number	890.3850   More FDA Info for this Regulation Number
Classification Product Code	IOR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/03/1996
Decision Date	05/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review