Medrad Interventional/Possis is one of 20373 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medrad Interventional/Possis - FDA 510(k) Cleared Devices
Recent clearances: FETCH 2 ASPIRATION CATHETER MODEL 109400-001, ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001
2
Total
2
Cleared
0
Denied
Medrad Interventional/Possis has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medrad Interventional/Possis Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medrad Interventional/Possis
2 devices