Medx, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Medx, Inc. has 8 FDA 510(k) cleared medical devices. Based in Wood Dale, US.
Historical record: 8 cleared submissions from 1987 to 2008. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Medx, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Nov 14, 2008
C-QUEST
Radiology
70d
Cleared
Dec 20, 2007
T-QUEST SYSTEM
Radiology
10d
Cleared
Aug 20, 2004
MEDX NUQUEST - INTECAM SPECT 37-75 SYSTEM
Radiology
43d
Cleared
Nov 30, 2001
GIOTTO IMAGE
Radiology
87d
Cleared
Feb 10, 2000
MEDX INTECAM INTERFACE
Radiology
86d
Cleared
Apr 12, 1989
D-SCOPE III
Radiology
156d
Cleared
Jun 18, 1987
D-SCOPE II AND D-SCOPE IIC
Radiology
16d
Cleared
Feb 26, 1987
SKAN D-SCOPE
Radiology
6d