FDA 510(k) Application Details - K051709

Device Classification Name	Wheelchair, Special Grade   More FDA Info for this Device
510(K) Number	K051709
Device Name	Wheelchair, Special Grade
Applicant	VIPAMAT TECHNOLOGIE 49 PLAIN STERRT NORTH ATTLEBORO, MA 02760 US Other 510(k) Applications for this Company
Contact	MARY MCNAMARA-CULLINANE Other 510(k) Applications for this Contact
Regulation Number	890.3880   More FDA Info for this Regulation Number
Classification Product Code	IQC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/27/2005
Decision Date	08/15/2005
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	N
Expedited Review