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
1444063280
Device Listing 1444063280
Listing Summary
#
Listing key
1444063280
Premarket submission
K131048
Device
LIDCO CNAP MODULE
Applicant
Lidco, Ltd.
Product code
DXG
Decision date
2013-08-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
55765
9617127
3001139253
Mathew Jimenez
1
N
2026-01-01
52 Discovery Irvine CA US 92618