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
1063796869
Device Listing 1063796869
Listing Summary
#
Listing key
1063796869
Premarket submission
K212145
Device
DR 800 with DSA, DR 800
Applicant
Agfa N.V.
Product code
JAA
Decision date
2021-08-31
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
221667
3001556265
3001556265
AGFA N.V.
1
N
2026-01-01
Septestraat 27 Mortsel Antwerpen BE B-2640