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
1070672126
Device Listing 1070672126
Listing Summary
#
Listing key
1070672126
Premarket submission
K901360
Device
LEVEEN PERITINEO-VENOUS SHUNT
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code
KPM
Decision date
1990-08-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
27609
2243072
2243072
BECTON DICKINSON
1
Y
2026-01-01
1 Becton Dr FRANKLIN LAKES NJ US 07417
161218
3010392988
3010392988
BD
1
N
2020-04-25
5859 Farinon Dr Ste 200 San Antonio TX US 78249