FDA 510(k) Application Details - K061721

Device Classification Name	Stretcher, Patient Restraint   More FDA Info for this Device
510(K) Number	K061721
Device Name	Stretcher, Patient Restraint
Applicant	EMERGENCY PRODUCTS AND RESEARCH 890 WEST MAIN STREET KENT, OH 44240 US Other 510(k) Applications for this Company
Contact	MARK MOEHLER Other 510(k) Applications for this Contact
Regulation Number	880.6900   More FDA Info for this Regulation Number
Classification Product Code	NZD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/19/2006
Decision Date	08/17/2006
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	N
Expedited Review