Ashva receives FDA 510(k) clearance for iMagic v 2.0 - Image management and reporting software for Ultrasound systems
Ashva Technologies Private Limited, has announced today that the United States Food & Drug Administration (FDA) has cleared iMagic version 2.0 for marketing in USA.Tweet
-- Ashva Technologies Private Limited, recognized as one of the leading PACS companies in India has announced today that the United States Food & Drug Administration (FDA) has cleared iMagic version 2.0 for marketing in USA. The iMagic software has been cleared for a variety of tasks including Ultrasound image archiving, manipulation, creation of template based reporting and distribution of images on to a media like a CD/DVD or printing them on standard Windows based printers.
Sunder Natrajan, CEO of Ashva Technologies Pvt Ltd states:
“We are very pleased to offer this additional value to our valued customers. Even though we have over 500 plus installations of iMagic in Asia, we strongly felt that we need to have the FDA clearance. The clearance is a testament to the fact that iMagic follows International standards of quality and usability. We believe that there is no other product in the market at this price range packed with so many features and with a FDA clearance. Ashva continues to strive to bring leading edge imaging software with features found only in the high end solutions and at prices which are very attractive to the end user and to our partners.”
Notes to Editor
In the field of Medical Technology, where cutting-edge solutions matter, Ashva has constantly strived to manage knowledge in the most efficient ways – developing functionality driven, cost-effective solutions for healthcare. Ashva in addition to the iMagic software for Ultrasound, offers PACS and PACS components like DICOM converter, viewer 2D and 3D, routers, etc. for applications in Radiology. To download a free 30 day demo copy of the iMagic software visit http://www.ashva.com/ or email firstname.lastname@example.org.