The U.S. Food and Drug Administration (FDA) issued the final guidance: Marketing Clearance of Diagnostic Ultrasound Systems and Transducers. This final guidance provides detailed recommendations for manufacturers seeking marketing clearance of diagnostic ultrasound systems and transducers.
Ambra Health announced an integration with Box to enable the sharing of medical imaging directly from within Box's cloud content management platform.
ImageGrid Mini is a feature-rich, reliable and cost-effective image management and workflow optimization solution ...
eHealth Saskatchewan plays a vital role in providing IT services to patients, health care providers, and partners such ...
Kevin Seals, M.D., University of California San Francisco (UCSF) Health, interventional radiology fellow, is working on ...
Konica Minolta Healthcare Americas, Inc. and the Emory Healthcare Innovation Hub recently formed a strategic partnership ...

SPONSORED CONTENT — EnsightTM 2.0 is the newest version of Enlitic’s data standardization software framework. Ensight is ...
At the Society for Imaging and Informatics in Medicine (SIIM) Annual Meeting in Aurora, Colo., Nuance Communications ...
While most women understand the importance of health screenings, an estimated 72 million have missed or postponed a ...
Nina Kottler, M.D., vice president of clinical operations, Radiology Partners, explains how the company developed its ...
Barco’s new remote radiology reading solution ensures dependable imaging when radiologists are working outside the ...
Fujifilm’s APERTO Lucent is a 0.4T mid-field, open MRI system addressing today’s capability and image quality needs ...
Use of 3-D mammography, an advanced form of breast cancer screening, has risen rapidly in recent years, according to ...
Way too often the technologies we thought would be wonderful turn out to be the bane of our existences. When that ...
Siemens Healthineers and Mentice AB announced the collaboration to fully integrate Mentice’s VIST Virtual Patient into the Artis icono angiography system from Siemens Healthineers. The VIST Virtual Patient thus becomes a fully integrated simulation solution for the angio suite, according to the companies. The global partnership between the two companies will allow interventional radiologists, neuroradiologists, and cardiologists to perform vascular and cardiac interventions on a virtual patient inside the angio-suite.
SPONSORED CONTENT — Fujifilm’s latest CT technology brings exceptional image quality to a compact and user- and patient ...
Artificial intelligence (AI) imaging solution form ClariPi Inc. has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its AI-based computed tomography (CT) denoising technology, ClariCT.AI.
Medical imaging is ripe for the picking. Here’s why. Imaging and information systems are becoming ever more connected ...
Lawrence Tanenbaum, M.D., Radnet vice president and chief technology officer, discusses some of the artificial ...
DOSIsoft announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market Planet Onco Dose software for its oncology and yttrium-90 (Y-90) microsphere SIRT 3-D dosimetry components.
Advanced visualization and artificial intelligence (AI) technology provider TeraRecon has successfully completed a U.S. Food and Drug Administration (FDA) regulatory review of its Northstar AI Results Explorer. TeraRecon said the technology and the determination are both firsts-of-kind in the medical imaging industry. Northstar is designed to work alongside the company’s EnvoyAI interoperability platform, which includes FDA-cleared third-party content listed on its EnvoyAI Exchange marketplace.
Bay Labs announced that new data on the company’s first-of-its-kind deep learning investigational guidance software will be presented at the upcoming American Society of Echocardiography (ASE) 30th Annual Scientific Sessions, June 21-25 in Portland, Ore.
Merit Medical Systems Inc. announced it has acquired Brightwater Medical Inc., based in Temecula, Calif. Brightwater Medical’s primary product, the ConvertX, is a single device used to replace a series of interventional radiology devices and procedures used to treat severe obstructions of the ureter.
Zebra Medical Vision announced it has received its third U.S. Food and Drug Administration (FDA) 510(k) clearance for the company's HealthICH product. The new clearance covers an artificial intelligence (AI) alert for intracranial hemorrhage (ICH), based on head computed tomography (CT) scans.