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
1334030625
Device Listing 1334030625
Listing Summary
#
Listing key
1334030625
Premarket submission
K090833
Device
SEGMENT
Applicant
Medviso
Product code
LLZ
Decision date
2009-05-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
126499
3008962159
3008962159
MEDVISO AB
1
N
2026-01-01
Griffelvagen 3 Lund Skane SE 224 67