Accuray, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accuray, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Accuray, Inc. has 10 FDA 510(k) cleared radiology devices. Based in Sunnyvale, US.
Historical record: 10 cleared submissions from 1999 to 2009.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Accuray, Inc.
10 devices
Cleared
Sep 18, 2009
CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
Radiology
78d
Cleared
May 01, 2009
MODIFICATION TO CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
Radiology
11d
Cleared
Oct 30, 2006
CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
Radiology
31d
Cleared
Aug 09, 2005
CYBERNIFE STEREOTACTIC RADIOSURGERY SYSTEM
Radiology
22d
Cleared
Jun 10, 2004
CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY
Radiology
24d
Cleared
Sep 03, 2003
CYBERKNIFE SYSTEM FOR STEROTACTIC RADIOSURGERY/RADIOTHERAPY
Radiology
35d
Cleared
Apr 22, 2002
MOTION TRACKING
Radiology
84d
Cleared
Aug 10, 2001
CYBERKNIFE SYSTEM
Radiology
128d
Cleared
Apr 19, 2000
THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1
Radiology
65d
Cleared
Jul 14, 1999
THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY
Radiology
203d