Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings.Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings.Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings.

Hologic Inc. announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its Quantra 2.2 Breast Density Assessment Software. The software enables clinicians to provide women with consistent breast density assessments during routine breast cancer screenings.

Head CT AI Augmented Screening

Infervision is introducing what it calls the first and only artificial intelligence (AI) platform to help radiologists detect and diagnose stroke faster, leading to patients getting life-saving treatment when time is of the essence. This new stroke detection solution is being introduced at the 2017 Radiological Society of North America (RSNA) conference, Nov. 26-Dec. 1 in Chicago.

November 27, 2017 — At the 103rd Scientific Assembly and Annual Meeting of the Radiological Society of North America (RSNA), Siemens Healthineers debuted GOKnee3D, a magnetic resonance imaging (MRI) application that drastically shortens the time required to perform comprehensive diagnostic exams of the knee. Currently, a typical knee examination can be roughly 20 minutes.

November 27, 2017 — Artificial intelligence (AI) startup Aidoc announced that it received CE (Conformité Européenne) marking for what it calls the world's first commercial head and neck deep learning medical imaging solution. CE marking allows for widespread commercialization of Aidoc's solution in Europe.

November 26, 2017 — Arterys Inc. announced the unveiling of their Arterys MICA platform at the 2017 Radiological Society of North America annual meeting (RSNA), Nov. 26-Dec. 1 in Chicago. Visitors to the Arterys Booth will be able to interact with a new portfolio of web-based artificial intelligence (AI) offerings supported by the platform.

Samsung Electronics debuted its OmniTom mobile 16-slice computed tomography (CT) scanner at the Radiological Society of North America (RSNA) 2017 Annual Meeting, Nov. 26-Dec. 1 in Chicago. OmniTom received 510(k) U.S. Food and Drug Administration (FDA) clearance for the U.S. market on Aug. 18 of this year.

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