Accuray, Inc.
Accuray, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2009.
Top product codes for Accuray, Inc.
Recent clearances by Accuray, Inc.
- K091999 — CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
- K091146 — MODIFICATION TO CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
- K062967 — CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
- K051941 — CYBERNIFE STEREOTACTIC RADIOSURGERY SYSTEM
- K041315 — CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY
- K032345 — CYBERKNIFE SYSTEM FOR STEROTACTIC RADIOSURGERY/RADIOTHERAPY
- K020294 — MOTION TRACKING
- K011024 — CYBERKNIFE SYSTEM
- K000478 — THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1
- K984563 — THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY
Data sourced from openFDA. This site is unofficial and independent of the FDA.