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
1915517116
Device Listing 1915517116
Listing Summary
#
Listing key
1915517116
Premarket submission
K780130
Device
BURETTE INTRAVENOUS ADMIN. SETS.
Applicant
Y
Product code
FPA
Decision date
1978-02-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
110332
1423507
3008002452
CAREFUSION 2200, INC.
1
Y
2026-01-01
75 North Fairway Drive Vernon Hills IL US 60061