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
1673609303
Device Listing 1673609303
Listing Summary
#
Listing key
1673609303
Premarket submission
K051901
Device
NIO 3MP-21
Applicant
Barcoview
Product code
LLZ
Decision date
2005-08-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
17234
9613188
3004455125
BARCO N.V.
1
N
2026-01-01
35 PRESIDENT KENNEDYPARK KORTRIJK West-Vlaanderen BE 8500