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
2072786806
Device Listing 2072786806
Listing Summary
#
Listing key
2072786806
Premarket submission
K141138
Device
SURFLASH SAFETY I.V. CATHETER
Applicant
Kofu Factory of Terumo Corp.
Product code
FOZ
Decision date
2014-05-30
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
256720
3012410077
3012410077
CAREFUSION
1
Y
2026-01-01
3750 Torrey View Court San Diego CA US 92130