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
1436718420
Device Listing 1436718420
Listing Summary
#
Listing key
1436718420
Premarket submission
K241608
Device
nordicMEDiVA
Applicant
Nordicneurolab AS
Product code
LLZ
Decision date
2024-06-28
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
68002
3006738448
3006738448
NORDICNEUROLAB AS
1
N
2026-01-01
MOLLENDALSVEIEN 1 BERGEN Hordaland NO 5009