Mediguide, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mediguide, Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Mediguide, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 3 cleared submissions from 2009 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mediguide, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mediguide, Ltd.
3 devices