FDA 510(k) Application Details - K032528

Device Classification Name	More FDA Info for this Device
510(K) Number	K032528
Device Name	BD ECLIPSE BIFURCATED NEEDLE
Applicant	BECTON DICKINSON & CO. 1 BECTON DR. FRANKLIN LAKES, NJ 07417-1885 US Other 510(k) Applications for this Company
Contact	PETER ZURLO Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	SCL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/15/2003
Decision Date	09/09/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review