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
1777063280
Device Listing 1777063280
Listing Summary
#
Listing key
1777063280
Premarket submission
K120573
Device
MEDART 620
Applicant
Medart A/S
Product code
GEX
Decision date
2012-06-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
171382
3010683226
3010683226
AdvaLight APS
1
N
2026-01-01
Industriparken 22 A Ballerup Hovedstaden DK DK-2750