Ashva Technologies Limited announced today that the United States Food & Drug Administration (FDA) has cleared the Edge PACS solution for marketing in USA. All of the Edge PACS components including Server, Web viewer & DICOM workstation have been awarded FDA 510(k).
Edge PACS has received FDA 510(k) clearance for diagnostic viewing and manipulating medical images. The Edge PACS can be fully integrated with an institution’s existing HIS or RIS providing access to reports for fully integrated electronic patient records.
Ashva’s Edge PACS demands minimal investment and its scale-ability enables the user to enjoy current needs and adapts to future requirements. Ashva has a collaborative/flexible approach towards installation & training thus enabling easier transition for customers. Ashva provides remote log-in for troubleshooting and frequent customer based product upgrades.
Sunder Natrajan, CEO of Ashva Technologies Pvt Ltd states:
"FDA 510(k) approval of the Edge PACS demonstrates Ashva's commitment to provide high quality products, developed under a stringent quality management system, for the benefit of our partners' product development and end user’s ease of use.”
About Ashva:
Ashva is a major OEM presence for radiology imaging solutions in Asia Pacific and one of the top 5 PACS companies in India as quoted by Frost & Sullivan report in 2007, Ashva technologies commenced its north American and European operations in the year 2007 to address markets which demand solutions that are feature rich yet affordable.
For further information on Edge PACS enterprise solution & Ashva, kindly visit – www.ashva.com. Or feel free to mail into marketing@ashvatech.com.
