Author: TechNation Magazine

GE HealthCare has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for MIM LesionID Pro[i], an innovative solution from its MIM software portfolio that transforms whole-body tumor burden analysis for PSMA PET/CT and SPECT/CT studies into a significantly simplified process.

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FDA

The FDA’s Center for Devices and Radiological Health’s (CDRH) mission is to protect and promote public health while supporting timely access to innovative, safe and effective medical devices and safe radiation-emitting products.

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Intelas, Compass Healthcare’s signature Healthcare Technology Management (HTM) brand, has launched TeamCHAMPS, a new mobile experience designed to simplify medical equipment service and strengthen day-to-day communication.

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