FDA 510(k) Application Details - K070268

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K070268
Device Name	Pump, Infusion
Applicant	CARDINAL HEALTH 303, INC. 10221 WATERIDGE CIR. SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	STACY L LEWIS Other 510(k) Applications for this Contact
Regulation Number	880.5725   More FDA Info for this Regulation Number
Classification Product Code	FRN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/29/2007
Decision Date	02/23/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review