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
1990199030
Device Listing 1990199030
Listing Summary
#
Listing key
1990199030
Premarket submission
K251363
Device
ProKnow DS
Applicant
Elekta Solutions AB
Product code
LLZ
Decision date
2025-10-08
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
228750
3015232217
3015232217
ELEKTA SOLUTIONS AB
1
N
2026-01-01
Hagaplan 4 STOCKHOLM SE 11368