Radiant Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Radiant Medical - FDA 510(k) Cleared Devices
6
Total
5
Cleared
0
Denied
Radiant Medical has 5 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 5 cleared submissions from 2002 to 2007. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Radiant Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Radiant Medical
6 devices
Cleared
Jun 01, 2007
REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM
Neurology
17d
Cleared
May 09, 2007
REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM
Neurology
30d
Cleared
Jan 08, 2007
REPRIEVE ENDOVASCULAR TEMPERATURE THERAPY SYSTEM
Neurology
60d
Cleared
Oct 28, 2004
RADIANT MEDICAL ENDOCATHETER TEMPERATURE PROBE
Cardiovascular
56d
Cleared
Mar 25, 2003
SETPOINT ENDOVASCULAR TEMPERATURE PROBE
Cardiovascular
89d
Cleared
Jun 11, 2002
SETPOINT ENDOVASCULAR TEMPERATURE MANAGEMENT SYSTEM
Neurology
309d