Mr Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DuoFLEX Coil Suite, DUOFLEX COIL SUITE (1.5T), MC 1504G-16R, 1.5T, 16-CHANNEL, MC 3004G-16R, 3.0T, 16-CHANNEL HEAD COIL
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mr Instruments, Inc. Radiology ✕
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