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
2045599470
Device Listing 2045599470
Listing Summary
#
Listing key
2045599470
Premarket submission
K103433
Device
F20
Applicant
Teknimed, S.A.
Product code
NDN
Decision date
2011-01-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
19024
9615788
3003854593
Barry Sands
1
N
2026-01-01
110 Haverhill Rd Ste 524 Amesbury MA US 01913