Abbott West Distribution Center

FDA Filings

This page includes the latest FDA filings for Abbott West Distribution Center. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3006604866
FEI Number3006604866
NameAbbott West Distribution Center
Owner & OperatorABBOTT LABORATORIES
Contact Address100 ABBOTT PARK RD. D-03Q3, AP52-1
Abbott Park IL 60064 US
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address42301 Zevo Drive
Temecula, CA 92590 US
Establishment TypeRepack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
Abbott West Distribution Center [ABBOTT LABORATORIES]
Xience Xpedition Coronary Drug-Eluting Stent System2011-11-01
Abbott West Distribution Center [ABBOTT LABORATORIES]
Xience Sierra2011-11-01
Abbott West Distribution Center [ABBOTT LABORATORIES]
Xience Prime2011-11-01
Abbott West Distribution Center [ABBOTT LABORATORIES]
Xience Alpine2011-11-01
Abbott West Distribution Center [ABBOTT LABORATORIES]
XIENCE XPEDITION RX Drug Eluting Stent System2011-11-01
Abbott West Distribution Center [ABBOTT LABORATORIES]
XIENCE XPEDITION OTW Drug Eluting Stent System2011-11-01
Abbott West Distribution Center [ABBOTT LABORATORIES]
Xience V2007-11-27
Abbott West Distribution Center [ABBOTT LABORATORIES]
Xience Nano2007-11-27
Abbott West Distribution Center [ABBOTT LABORATORIES]
XIENCE V, RX Drug Eluting Stent System2007-11-27
Abbott West Distribution Center [ABBOTT LABORATORIES]
XIENCE V, OTW Drug Eluting Stent System2007-11-27
Abbott West Distribution Center [ABBOTT LABORATORIES]
XIENCE V Everolimus Eluting Coronar2007-11-27

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