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
2048448235
Device Listing 2048448235
Listing Summary
#
Listing key
2048448235
Premarket submission
K101114
Device
ADVANCIS ACTIVON TUBE
Applicant
Advancis Medical
Product code
FRO
Decision date
2011-07-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
45880
2435946
1000137528
DUKAL LLC
1
Y
2026-01-01
2 Fleetwood Ct. Ronkonkoma NY US 11779