Roche's momentum in digital pathology continues with FDA clearance on its high-volume slide scanner
Roche's momentum in digital pathology continues with FDA clearance on its high-volume slide scanner |
[09-January-2025] |
TUCSON, Ariz., Jan. 9, 2025 /PRNewswire/ -- Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today that its whole slide imaging system, Roche Digital Pathology Dx, has received an additional 510(k) clearance from the United States Food and Drug Administration (FDA). This clearance modifies the one Roche received on June 14, 2024 for Roche Digital Pathology Dx, which includes the VENTANA DP 200 slide scanner, Roche's digital pathology workflow software and a display, and now adds the VENTANA DP 600 slide scanner. "The VENTANA DP 600 high-capacity slide scanner creates high-resolution, digital images of stained tissue samples that help clinicians diagnose cancer and determine a patient's treatment," said Jill German, Head of Pathology Lab for Roche Diagnostics. "The recent FDA clearances continue our momentum to advance the pathology lab's digital transformation and reinforce our commitment to enhance patient care and healthcare efficiency through streamlining the digital workflow." The VENTANA DP 600 has 40 times the capacity of the VENTANA DP 200 and uses the same scanning technology, providing pathologists with consistent, high quality images from both systems. Roche Digital Pathology Dx now includes the VENTANA DP 200 slide scanner, the VENTANA DP 600 slide scanner, Roche's digital pathology workflow software and a display. Roche Digital Pathology Dx is intended to aid the pathologist in reviewing and interpreting digital images of scanned pathology slides prepared from formalin-fixed paraffin-embedded (FFPE) tissue when diagnosing patients. About Roche Digital Pathology About Roche For over 125 years, sustainability has been an integral part of Roche's business. As a science-driven company, our greatest contribution to society is developing innovative medicines and diagnostics that help people live healthier lives. Roche is committed to the Science Based Targets initiative and the Sustainable Markets Initiative to achieve net zero by 2045. Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan. For more information, please visit www.roche.com. All trademarks used or mentioned in this release are protected by law. Roche Media Relations Jo Lynn Garing, +1 317-363-7286 or jo_lynn.garing@roche.com Amberly Peterson, +1 317-478-2210 or amberly.peterson@roche.com View original content to download multimedia:https://www.prnewswire.com/news-releases/roches-momentum-in-digital-pathology-continues-with-fda-clearance-on-its-high-volume-slide-scanner-302338378.html SOURCE Roche | ||
Company Codes: Swiss:ROG, OTC-PINK:RHHBY, Swiss:RO, OTC-BB:RHHBY, OTC-QX:RHHBY, OtherOTC:RHHBY |