Roche’s move into the digital pathology category has been boosted by FDA approval of a lab instrument ... The latest development revolves around 510(k) approval of the Ventana DP 200 for ...
The FDA has granted 510(k) clearance to AI Optics’ Sentinel Camera, a handheld retinal imaging system that captures ...
Christophe Gardella, Ph.D., Chief Technical Officer, BrightHeart BrightHeart is the Paris-based manufacturer of the AI-based software. In November 2024, BrightHeart obtained FDA 510(k) approval for ...
RapidAI, the global leader in AI-driven medical imaging analysis and coordinated care, has received FDA 510(k) clearance for Lumina 3D™ by RapidAI—an industry-first, automated 3D imaging ...
Robotic gait training was provided to participants in the RE+SOC Group during stroke rehabilitation at an inpatient rehabilitation hospital through a commercially available, FDA class 2 approved ...
For the first time in two decades, the Food and Drug Administration (FDA) has approved a new class of medication that provides an alternative to addictive opioids for patients looking to manage ...
NEW YORK (AP) — Free agent pitcher Jeison Pena was suspended for 80 games on Friday under baseball’s minor league drug program and Colorado Rockies pitcher Ulises Reyes for 56 games under the ...
(CNN) – The U.S. Food and Drug Administration approved the first new type of pain medication in more than two decades, and it’s not an opioid. The drug is suzetrigine under the brand name ...
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