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
1945104144
Device Listing 1945104144
Listing Summary
#
Listing key
1945104144
Premarket submission
K955434
Device
ACCESS FOLATE ASSAY (MODIFICATION)
Applicant
Beckman Coulter, Inc.
Product code
CGN
Decision date
1996-01-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
5265
2122870
2122870
BECKMAN COULTER, INC.
1
Y
2026-01-01
1000 LAKE HAZELTINE DR. CHASKA MN US 55318