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
1272660513
Device Listing 1272660513
Listing Summary
#
Listing key
1272660513
Premarket submission
K031825
Device
C.CAM
Applicant
Danish Diagnostic Development A/S
Product code
KPS
Decision date
2003-06-20
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
324090
3030186509
3030186509
X3D APS
1
N
2026-01-01
Oldenvej 33 Kvistgaard Hovedstaden DK 3490