Romedex International Srl is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Romedex International Srl - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Romedex International Srl has 2 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 2 cleared submissions from 2010 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Romedex International Srl Filter by specialty or product code using the sidebar.
Romedex International Srl — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jan 27, 2015
NAUTILUS DELTA
General Hospital
223d
Cleared
Jul 15, 2010
EVGUIDE TIP LOCATION SYSTEM
General Hospital
219d