FDA 510(k) Application Details - K960466

Device Classification Name	Set, I.V. Fluid Transfer   More FDA Info for this Device
510(K) Number	K960466
Device Name	Set, I.V. Fluid Transfer
Applicant	ABBOTT LABORATORIES 200 ABBOTT PARK RD. D-389, BLDG AP30 ABBOTT PARK, IL 60064-3500 US Other 510(k) Applications for this Company
Contact	JILL N SACKETT Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	LHI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/02/1996
Decision Date	05/29/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review