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
1946736143
Device Listing 1946736143
Listing Summary
#
Listing key
1946736143
Premarket submission
K991010
Device
ACP
Applicant
Abbott Diagnostics Mfg., Inc.
Product code
CKB
Decision date
1999-05-19
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
233388
3005333358
3005333358
ABBOTT LABORATORIES
1
N
2026-01-01
Conway Park 675 North Field Drive Lake Forest IL US 60045
236886
3016438761
3016438761
ABBOTT LABORATORIES
1
Y
2026-01-01
1915 Hurd Drive Irving TX US 75038