Abbvie Medical Device Center

FDA Filings

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

FDA Registration(s)
Registration Number3010757606
FEI Number3010757606
NameAbbVie - Medical Device Center
Owner & OperatorAbbVie Inc.
Contact Address1 N. Waukegan Rd J23
North Chicago IL 60064 US
Official Correspondent
  • Mary B Mathieu
  • 01-847-9380015-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1675 Lakeside Dr
Waukegan, IL 60085 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198

FDA Filings

Device
Company
DeviceDate
AbbVie - Medical Device Center [AbbVie Inc.]
Abbvie Lightweight Vest2016-06-15
AbbVie - Medical Device Center [AbbVie Inc.]
AbbVie Snug Vest2016-06-15
AbbVie - Medical Device Center [AbbVie Inc.]
AbbVie Hip Pack2016-06-15
AbbVie - Medical Device Center [AbbVie Inc.]
AbbVie Cross Body Pack2016-06-15
AbbVie - Medical Device Center [AbbVie Inc.]
AbbVie Chest Pack2016-06-15
AbbVie - Medical Device Center [AbbVie Inc.]
AbbVie NJ2015-02-04
AbbVie - Medical Device Center [AbbVie Inc.]
AbbVie J2015-01-21
AbbVie - Medical Device Center [AbbVie Inc.]
AbbVie PEG2015-01-21

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