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
2032018229
Device Listing 2032018229
Listing Summary
#
Listing key
2032018229
Premarket submission
K161508
Device
Ceruloplasmin
Applicant
Beckman Coulter Ireland, Inc.
Product code
DDB
Decision date
2017-01-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
5259
2050012
2050012
BECKMAN COULTER, INC.
1
Y
2026-01-01
250 S Kraemer Blvd BREA CA US 92821
107181
9680746
1000206808
Ian Pilcher
1
N
2026-01-01
1000 Lake Hazeltine Dr Chaska MN US 55318