Pro-Tronics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pro-Tronics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Wood Dale, US.
Historical record: 5 cleared submissions from 1989 to 1995. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Pro-Tronics, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Apr 11, 1995
MOBIL C-ARM, REGURBISHED, VARIOUS MODELS
Radiology
49d
Cleared
Mar 14, 1995
GENERAL ELECTRIC AMX 110, AMX II AND AMX 3
Radiology
183d
Cleared
Jul 02, 1990
GENERAL ELECTRIC AMX 3
Radiology
20d
Cleared
May 03, 1989
GENERAL ELECTRIC AMX 110
Radiology
61d
Cleared
May 01, 1989
GENERAL ELECTRIC AMX II
Radiology
59d