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
1076585164
Device Listing 1076585164
Listing Summary
#
Listing key
1076585164
Premarket submission
K142745
Device
125mL CT Syringe
Applicant
Coeur, Inc.
Product code
DXT
Decision date
2015-04-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
56550
1038185
1038185
COEUR, INC.(A WHOLLY OWNED SUBSIDIARY OF ILLINOIS TOOL WORKS INC.)
1
N
2026-01-01
209 Creekside Dr WASHINGTON NC US 27889