FDA 510(k) Application Details - K020737

Device Classification Name	Wheelchair, Mechanical   More FDA Info for this Device
510(K) Number	K020737
Device Name	Wheelchair, Mechanical
Applicant	MOVINGPEOPLE.NET 500 NORTINCH DR. TORONTO, ONTARIO M3N 1Y4 CA Other 510(k) Applications for this Company
Contact	PEGGY SPILIADIS 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	03/06/2002
Decision Date	03/21/2002
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	Y
Expedited Review