Mr Instruments, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Mr Instruments, Inc. has 7 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 7 cleared submissions from 2004 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Mr Instruments, Inc. Filter by specialty or product code using the sidebar.
7 devices
Cleared
Nov 28, 2017
DuoFLEX Coil Suite
Radiology
43d
Cleared
Jul 25, 2013
DUOFLEX COIL SUITE (1.5T)
Radiology
132d
Cleared
Mar 29, 2011
MC 1504G-16R, 1.5T, 16-CHANNEL, MC 3004G-16R, 3.0T, 16-CHANNEL HEAD COIL
Radiology
27d
Cleared
Apr 02, 2008
TEM 3002G- HN DUAL TUNE HEAD COIL
Radiology
9d
Cleared
Oct 30, 2007
MC 3003G-32R HEAD COIL
Radiology
14d
Cleared
Aug 19, 2005
TEM 3000 HEAD COIL
Radiology
7d
Cleared
Apr 23, 2004
TEM 3000 HEAD COIL
Radiology
11d