Philips (NYSE:PHG) announced today that it received FDA 510(k) clearance for its AI-powered Spectral CT Verida system.
Last month, Philips obtained FDA clearance for DeviceGuide, an AI-based software designed to provide physicians with ...
Designed specifically for use in radiation oncology, new Spectral CT 7500 RT enables personalized radiation therapy planning to deliver better care for more cancer patients Spectral CT 7500 RT ...
CE Marked and 510(k) pending, Rembra’s advanced image reconstruction technology delivers up to 106 images per second [1] and a high throughput of up to 270 patients per day [2] to support faster ...
Koninklijke Philips PHG announced the launch of the Philips CT 5300 system, which is intended to be used for screening, interventional treatments and diagnostics. It is outfitted with cutting-edge AI ...
Philips has secured an FDA clearance for what it describes as the world’s first imager to combine spectral CT with four-dimensional captures in a single scan, with a design specifically targeting the ...
Philips has received clearance from the FDA for its artificial-intelligence-powered MRI platform geared toward head and neck cancers. Dubbed MRCAT, for MR for Calculating ATtenuation, the application ...
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