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
1587068787
Device Listing 1587068787
Listing Summary
#
Listing key
1587068787
Premarket submission
K233030
Device
BoneMRI
Applicant
Mriguidance B.V.
Product code
QIH
Decision date
2024-03-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
319454
3027986210
3027986210
MRIGUIDANCE B.V.
1
N
2026-01-01
Maliesingel 23 Utrecht NL 3581BG