FDA 510(k) Application Details - K113598

Device Classification Name	Stretcher, Wheeled   More FDA Info for this Device
510(K) Number	K113598
Device Name	Stretcher, Wheeled
Applicant	STRYKER MEDICAL 3800 E. CENTRE AVE. PORTAGE, MI 49002 US Other 510(k) Applications for this Company
Contact	RENATA SILA Other 510(k) Applications for this Contact
Regulation Number	880.6910   More FDA Info for this Regulation Number
Classification Product Code	FPO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/2011
Decision Date	12/20/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review