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
1682649831
Device Listing 1682649831
Listing Summary
#
Listing key
1682649831
Premarket submission
K110850
Device
K-PACK II NEEDLE- 27G & 30G THIN WALL
Applicant
Terumo Europe N.V.
Product code
FMI
Decision date
2011-06-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
176311
1000118068
1000118068
GALDERMA LABORATORIES, L.P.
1
Y
2026-01-01
14600 Heritage Pkwy Fort Worth TX US 76177