THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY— 510(k) K984563

Name: FDA 510(k) clearance K984563
Creator: U.S. Food and Drug Administration
Published: 1999-07-14

Substantially Equivalent

Accuray, Inc.

FDA 510(k) clearance K984563 for THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY, Substantially Equivalent on 1999-07-14. Applicant: Accuray, Inc.. Device class: 2.

Clearance details

Applicant: Accuray, Inc.
Product code: Code IWB
Device class: Class 2
Regulation: 21 CFR 892.5750
Advisory panel: Radiology
Date received: 1998-12-23
Decision date: 1999-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.