FDA 510(k) Application Details - K020933

Device Classification Name	Elevator, Wheelchair   More FDA Info for this Device
510(K) Number	K020933
Device Name	Elevator, Wheelchair
Applicant	GARAVENTA ACCESSIBILITY BOX 1769 BLAIN, WA 98231-1769 US Other 510(k) Applications for this Company
Contact	NORM COOPER Other 510(k) Applications for this Contact
Regulation Number	890.3930   More FDA Info for this Regulation Number
Classification Product Code	ING Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/22/2002
Decision Date	04/04/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review