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
1889981831
Device Listing 1889981831
Listing Summary
#
Listing key
1889981831
Premarket submission
K220590
Device
aPROMISE X
Applicant
Exini Diagnostics AB
Product code
LLZ
Decision date
2022-04-29
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
146500
3010146120
3010146120
EXINI DIAGNOSTICS AB
1
N
2026-01-01
Ideon Science Park Scheelevagen 27 LUND Skane SE SE-223 70