Bruker Medical Imaging, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bruker Medical Imaging, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Bruker Medical Imaging, Inc. has 7 FDA 510(k) cleared medical devices. Based in Lisle, US.
Historical record: 7 cleared submissions from 1989 to 1992. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Bruker Medical Imaging, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bruker Medical Imaging, Inc.
7 devices
Cleared
Mar 13, 1992
MODIFIED MAGNETIC RESONANCE IMAGING SYTEM MOD. R28
Radiology
86d
Cleared
Nov 29, 1991
MAG RES IMAG SYST/BRUKER MODEL R28 WHOLE BODY SCAN
Radiology
116d
Cleared
Nov 13, 1990
BRUKER R-28,HEAD AND CHEST ANGIOGRAPHY IMAGING ADD
Radiology
92d
Cleared
Apr 30, 1990
BRUKER R28 WHOLE-BODY MR SCANNER
Radiology
117d
Cleared
Mar 09, 1990
MAGNETIC RESONANCE SYSTEM MODEL BMT-1100
Radiology
190d
Cleared
Nov 15, 1989
1989 SOFTWARE REVISION TO THE BMT-1100
Radiology
114d
Cleared
Jun 23, 1989
MAGNETIC RESONANCE SYSTEM, MODEL BMT 1100,MODIFIED
Radiology
92d