Kermath Mfg. Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Kermath Mfg. Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1977 to 1987. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Kermath Mfg. Corp. Filter by specialty or product code using the sidebar.
5 devices
Cleared
May 12, 1987
T.O.P. 2000 (TOMOGRAPHIC ORIENTATED PLANNING)
Radiology
111d
Cleared
Nov 05, 1981
KERMATH THERAPY SIMULATOR
Radiology
38d
Cleared
Sep 16, 1981
KERMATH L/C ARM
Radiology
29d
Cleared
Jun 12, 1981
KERMATH RADIOGRAPHIC HEAD STAND
Radiology
39d
Cleared
Aug 25, 1977
VERSATOME
Radiology
13d