Mr Instruments Inc

FDA Filings

This page includes the latest FDA filings for Mr Instruments Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3003852428
FEI Number3003852428
NameMR INSTRUMENTS, INC.
Owner & OperatorMR Instruments, Inc.
Contact Address5610 Rowland Road, Suite 145
Minnetonka MN 55343 US
Official Correspondent
  • Robert Bushey
  • x-952-7461435-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address5610 Rowland Road, Suite 145
Minnetonka, MN 55343 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
MR INSTRUMENTS, INC.
DuoFLEX Coil Suite2018-01-10
MR Instruments, Inc
DuoFLEX Coil Suite2017-11-28
MR INSTRUMENTS, INC.
DuoFLEX Coil Suite (1.5T)2016-06-21
MR INSTRUMENTS, INC.
MC3003G-32R Head Coil2016-06-15
MR INSTRUMENTS, INC.
DUOFLEX COIL SUITE (1.5T)2013-07-25
MR INSTRUMENTS, INC.
MC 1504G-16R, 1.5T, 16-CHANNEL, MC 3004G-16R, 3.0T, 16-CHANNEL HEAD COIL2011-03-29
MR INSTRUMENTS, INC.
MC 3003G-32R HEAD COIL2007-10-30
MR INSTRUMENTS INC.
TEM 3000 HEAD COIL2005-08-19
MR INSTRUMENTS, INC.
TEM 3000 HEAD COIL2004-04-23

Related Finance Registrations
SEC0001376983MR INSTRUMENTS INC
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