Medical Device Manufacturer · US , Sunnyvale , CA

Accuray, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1999
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
1-10 of 10
Cleared Sep 18, 2009
CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
K091999 · IYE
Radiology · 78d
Cleared May 01, 2009
MODIFICATION TO CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
K091146 · MUJ
Radiology · 11d
Cleared Oct 30, 2006
CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
K062967 · MUJ
Radiology · 31d
Cleared Aug 09, 2005
CYBERNIFE STEREOTACTIC RADIOSURGERY SYSTEM
K051941 · MUJ
Radiology · 22d
Cleared Jun 10, 2004
CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY
K041315 · IYE
Radiology · 24d
Cleared Sep 03, 2003
CYBERKNIFE SYSTEM FOR STEROTACTIC RADIOSURGERY/RADIOTHERAPY
K032345 · MUJ
Radiology · 35d
Cleared Apr 22, 2002
MOTION TRACKING
K020294 · IYE
Radiology · 84d
Cleared Aug 10, 2001
CYBERKNIFE SYSTEM
K011024 · IYE
Radiology · 128d
Cleared Apr 19, 2000
THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1
K000478 · IWB
Radiology · 65d
Cleared Jul 14, 1999
THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY
K984563 · IWB
Radiology · 203d
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