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
1193251364
Device Listing 1193251364
Listing Summary
#
Listing key
1193251364
Premarket submission
K163334
Device
LiDCOunity v2 Hemodynamic Monitor
Applicant
Lidco, Ltd.
Product code
DXG
Decision date
2017-06-05
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