FDA Clears Siemens CT Scanners for Low-Dose Lung Cancer Screening

Siemens now offers the industry's most comprehensive approach to low-dose lung cancer screening


Siemens has also launched a unique mobile imaging solution for lung cancer screening

The United States Food and Drug Administration (US FDA) has cleared Siemens Healthcare's SOMATOM computed tomography (CT) systems for low-dose lung cancer screening.

From the SOMATOM Scope 16-slice CT system to the ultra-premium SOMATOM Force, Siemens now makes low-dose lung cancer screening broadly available to its customers.

"Lung cancer screening represents one of the most significant opportunities to improve population health through earlier detection and improved follow-up opportunities for high-risk patients," said Mr David Pacitti, president of Siemens Healthcare North America. "That's why Siemens pursued the most expansive indication for lung cancer screening, bringing this valuable tool to all varieties of our current SOMATOM CT scanners."

The indication for low-dose lung cancer screening is available for the following CT systems: SOMATOM Force, SOMATOM Definition Flash, SOMATOM Definition Edge, SOMATOM Definition AS/AS+, SOMATOM Perspective, SOMATOM Scope, and the SOMATOM Emotion.

Siemens' portfolio of CT systems offers solutions for low-dose lung imaging from screening to detection to diagnosis. With its FAST (Fully Assisting Scanner Technologies) features, Siemens optimizes CT acquisition by reducing user variability. With FAST Planning, technologists can set an optimum range for scan settings that avoids cut-offs or excessive radiation.

Its CARE (Combined Applications to Reduce Exposure) feature delivers a consistent, reproducible approach to optimizing radiation dose in scan parameters that supports efficient clinical workflow. Features in the SOMATOM portfolio also aid the radiologist in reporting dose and sharing findings within the interdisciplinary lung cancer team.


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