LINACWATCH: FDA 510k clearance

November 5, 2017

End of October 2017, FDA grants LINACWATCH 510k clearance

QUALIFORMED, European leader in innovative software for quality assurance (QA) in radiation oncology and medical imaging, is pleased to announce that its LINACWATCH software has received U.S. market clearance as a Class II medical device from the Food and Drug Administration (FDA).


LINACWATCH is an effective, comprehensive yet simple solution to automatically analyse in real time and running in the background, the beam

just delivered by the treatment machines. 


LINACWATCH is an autonomous system fully integrated into the patient workflow which permanently and deeply follows the LINAC during the treatments.


For all these reasons LINACWATCH increases considerably and simply the patient safety.



Visit our LINACWATCH webpage for more information! 


Your brochure request has been added to your Download Cart.


At the end of your visit:


  • Please click the "YOUR DOWNLOADS" button at the top right,
  • Complete the form and SEND it.


You will get the documents shortly by email.