Trireme Medical, Inc. is one of 18904 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trireme Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CHOCOLATE PTCA BOLLOON CATHETER, CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.014 GUIDE WIRE, CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.018, CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.014 GUIDE WIRE, CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.18 G
Trireme Medical, Inc. has 12 FDA 510(k) cleared cardiovascular devices. Based in Pleasanton, US.
Historical record: 12 cleared submissions from 2010 to 2014.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services, Citech and Regulatory Technology Services, LLC.