FDA 510(k) Application Details - K090256

Device Classification Name	Wheelchair, Standup   More FDA Info for this Device
510(K) Number	K090256
Device Name	Wheelchair, Standup
Applicant	DAVISMADE, INC. 2511 DAVISON RD FLINT, MI 48506 US Other 510(k) Applications for this Company
Contact	DANIEL DAVIS Other 510(k) Applications for this Contact
Regulation Number	890.3900   More FDA Info for this Regulation Number
Classification Product Code	IPL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/02/2009
Decision Date	07/06/2009
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