Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1867525031
Device Listing 1867525031
Listing Summary
#
Listing key
1867525031
Premarket submission
K120863
Device
WHOLEY GUIDE WIRE SYSTEM
Applicant
Covidien, LLC
Product code
DQX
Decision date
2012-04-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
52258
2183870
2183870
ev3, Inc.
1
N
2026-01-01
4600 Nathan Lane North Plymouth MN US 55442