FDA 510(k), K062967, CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM

FDA 510(k), K062967, CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM

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510(K) Number: K062967
Device Name: CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
Manufacturer:
Device Classification Name: System, Planning, Radiation Therapy Treatment
Regulation Number: 892.5050
Classification Product Code: MUJ
Date Received: 09/29/2006
Decision Date: 10/30/2006
Regulation Medical Specialty: Radiology
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