FDA 510(k) Application Details - K122206

Device Classification Name	More FDA Info for this Device
510(K) Number	K122206
Device Name	GARAVENTA X3 INCLINED PLATFORM LIFT
Applicant	GARAVENTA (CANADA) LTD [DBA GARAVENTA LIFT] 845 ARONSON LAKE COURT ROSWELL, GA 30075 US Other 510(k) Applications for this Company
Contact	JAY MANSOUR Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PCE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/25/2012
Decision Date	03/21/2013
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