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
1970146654
Device Listing 1970146654
Listing Summary
#
Listing key
1970146654
Premarket submission
K040915
Device
MAGNITUDE 3150M MRI PATIENT MONITOR, MODEL 3150M
Applicant
Invivo Research, Inc.
Product code
MWI
Decision date
2004-09-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
1229
1051786
1051786
INVIVO CORPORATION
1
N
2026-01-01
12151 Research Pkwy Orlando FL US 32826