Dorsavi, Ltd. is one of 147 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Dorsavi, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Dorsavi, Ltd. has 2 FDA 510(k) cleared medical devices. Based in East Melbourne, AU.
Historical record: 2 cleared submissions from 2015 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Dorsavi, Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mjrac and Pushmed, LLC.
FDA 510(k) Regulatory Record - Dorsavi, Ltd.
2 devices