FDA 510(k) Application Details - K032880

Device Classification Name	Transport, Patient, Powered   More FDA Info for this Device
510(K) Number	K032880
Device Name	Transport, Patient, Powered
Applicant	SUMMIT LIFTS, INC. 7300 W. 110TH STREET SUITE 260 OVERLAND PARK, KS 66210 US Other 510(k) Applications for this Company
Contact	KENT PERRY Other 510(k) Applications for this Contact
Regulation Number	890.5150   More FDA Info for this Regulation Number
Classification Product Code	ILK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/15/2003
Decision Date	11/10/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	PM - Physical Medicine
Review Advisory Committee	PM - Physical Medicine
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review