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
1899310127
Device Listing 1899310127
Listing Summary
#
Listing key
1899310127
Premarket submission
K060637
Device
DENFIL FLOW
Applicant
Vericom Co., Ltd.
Product code
EBF
Decision date
2006-03-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
59141
3003449480
3003449480
ELIZABETH KIM
1
N
2026-01-01
22541 Aspan St. Suite A Lake Forest CA US 92630