Nashua, N.H.-based iCAD recently announced that its PowerLook Tomo Detection received FDA premarket approval. PowerLook Tomo Detection is a concurrent-read, computer-aided detection solution for digital breast 3D tomosynthesis and is the latest innovation available on the PowerLook Breast Health Solutions platform.
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What do HTM professionals need to know about battery use, battery maintenance, and battery purchasing? A clinical engineer and others divulge all in April’s cover story. Don’t miss out on this informative article.
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Neonatal care equipment manufacturers’ interest in offering high-end, technology-integrated, home-based infant care and neonatal solutions mirrors the healthcare industry’s shift toward value-based care, according to a report from market research firm Frost & Sullivan.
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Recent innovations have enabled biomedical test instruments to function more quickly, accurately, and cost-effectively, in addition to enhancing the capture, storage, traceability, and interpretation of critical data. In this article, 24×7 correspondent Ray Pelosi explores the latest advancements in test equipment and discusses how they affect HTM professionals. Don’t miss out.
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In order to reduce the lag time between manufacturer action and FDA posting, the FDA announced in January that it would begin posting product recalls in the Medical Device Recall database before the agency’s own classification procedure ran its course. It will be a marked improvement from how things have been in the past, maintains biomedical expert William Hyman, ScD.
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