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
1787579430
Device Listing 1787579430
Listing Summary
#
Listing key
1787579430
Premarket submission
K172200
Device
3880 MRI Patient Monitoring System
Applicant
Iradimed Corporation
Product code
MWI
Decision date
2017-10-25
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
64695
3005053560
3005053560
IRADIMED CORPORATION
1
N
2026-01-01
12705 Ingenuity Dr Orlando FL US 32826