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
1498300620
Device Listing 1498300620
Listing Summary
#
Listing key
1498300620
Premarket submission
K981758
Device
ALBG
Applicant
Abbott Laboratories
Product code
CIX
Decision date
1998-06-12
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