GE HealthCare has announced that View, the powerful viewer within the Genesis™ Radiology Workspace, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA).
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QT Imaging Holdings Inc. has announced receipt of U.S. Food and Drug Administration (FDA) 510(k) clearance for an updated configuration of its Breast Acoustic CT scanner, the Company’s 3D ultrasound tomographic breast imaging system.
Harrison.ai has announced FDA 510(k) clearance for acute infarct triage on non-contrast CT Brain. Acute infarct is one of the…
Fujitsu Limited and DT-Axis Co., Ltd. today announced the commencement of a collaboration aimed at advancing digital health. The two…
FUJIFILM Healthcare Americas Corporation will showcase how its latest AI-powered enterprise imaging solutions are enabling healthcare organizations to enhance workflows…
Medimaps Group S.A., a global leader in AI-driven bone microarchitecture imaging solutions, and Radiobotics ApS, a leader in AI-powered MSK…
GE HealthCare and UCSF Health have announced a 10-year Care Alliance collaboration focused on implementing advanced imaging and strengthening care delivery across the health system.
GE HealthCare has announced a new approximately $35 million expansion to a previous contract with the Biomedical Advanced Research and Development Authority (BARDA), part of the Administration for Strategic Preparedness and Response (ASPR) within the U.S. Department of Health and Human Services (HHS).
ACIST Medical Systems Inc., a Bracco Group company and a global leader in advanced contrast management technologies, today announced the…
Median Technologies has received FDA 510(k) clearance for eyonis LCS, its AI/ML-powered computer-aided detection and diagnosis (CADe/CADx) Software as a Medical Device intended for lung cancer screening.
