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
2046232688
Device Listing 2046232688
Listing Summary
#
Listing key
2046232688
Premarket submission
K980987
Device
BECTON DICKINSON SYRINGE
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code
FMF
Decision date
1998-06-11
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
152269
3010041511
3010041511
Teleflex LLC (NADC)
1
Y
2026-01-01
11245 N Distribution Cove Olive Branch MS US 38654