FDA 510(k) Application Details - K141474

Device Classification Name	More FDA Info for this Device
510(K) Number	K141474
Device Name	BECTON DICKINSON INTELLIPORT SYSTEM
Applicant	BECTON DICKINSON & CO. 11665 AVENA PLACE, SUITE 203 SAN DIEGO, CA 92128 US Other 510(k) Applications for this Company
Contact	DANIEL OLIVIER Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PHC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/03/2014
Decision Date	12/18/2014
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