FDA 510(k) Application Details - K091881

Device Classification Name	Elevator, Wheelchair   More FDA Info for this Device
510(K) Number	K091881
Device Name	Elevator, Wheelchair
Applicant	HARMAR SUMMIT LLC 2075 47TH STREET SARASOTA, FL 34234 US Other 510(k) Applications for this Company
Contact	KEVIN KAMINSKI 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	06/24/2009
Decision Date	07/01/2009
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