Skanray Technologies Pvt, Ltd. is one of 136 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Skanray Technologies Pvt, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Mysore, IN.
Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Skanray Technologies Pvt, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Smith Assoicates and Elexes.
FDA 510(k) Regulatory Record - Skanray Technologies Pvt, Ltd.
2 devices