Read more

October 18, 2021
1 min read
Save

FDA announces 510(k) clearance of photon-counting CT imaging device

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

The FDA has granted 510(k) clearance to Siemens Medical Solutions Inc. for the Siemens Naeotom Alpha, a new advancement in diagnostic CT imaging, according to a company press release.

The Naeotom Alpha is designed with photon-counting technology, which uses individual X-ray photons to provide physicians and trained staff with detailed information to aid in the diagnosis, treatment and planning of radiation therapy, according to the release.

“Computed tomography is an important medical imaging tool that can aid in diagnosing disease, trauma or abnormality; planning and guiding interventional or therapeutic procedures; and monitoring the effectiveness of certain therapies,” Laurel Burk, PhD, assistant director of diagnostic X-ray systems for the FDA’s Center for Devices and Radiological Health, said in the release. “Today’s action represents the first major new technology for computed tomography imaging in nearly a decade and underscores the FDA’s efforts to encourage innovation in areas of scientific and diagnostic progress,” Burk added.