FDA 510(k) Application Details - K102088

Device Classification Name	Elevator, Wheelchair   More FDA Info for this Device
510(K) Number	K102088
Device Name	Elevator, Wheelchair
Applicant	THYSSENKRUPP CETECO SRL VIA S.CANNIZZARO, 2 PISA 56121 IT Other 510(k) Applications for this Company
Contact	FABRIZIO FEDELE 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	07/26/2010
Decision Date	10/20/2010
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