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
1096718059
Device Listing 1096718059
Listing Summary
#
Listing key
1096718059
Premarket submission
K223432
Device
Vassallo GT 018 Hybrid
Applicant
Filmecc Co., Ltd.
Product code
DQX
Decision date
2023-03-09
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17
1016427
1016427
Cordis US Corp.
1
Y
2026-01-01
14201 N.W. 60TH AVE. Miami Lakes FL US 33014