FDA 510(k) Application Details - K071400

Device Classification Name	Stopcock, I.V. Set   More FDA Info for this Device
510(K) Number	K071400
Device Name	Stopcock, I.V. Set
Applicant	CARDINAL HEALTH, ALARIS PRODUCTS 10221 WATERIDGE CIRCLE SAN DIEGO, CA 92121-2772 US Other 510(k) Applications for this Company
Contact	STACY L LEWIS Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FMG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/21/2007
Decision Date	12/14/2007
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