Paragonix Technologies

Paragonix Technologies — FDA 510(k) Submissions

Paragonix Technologies has submitted 5 FDA 510(k) premarket notifications since 2018, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Perfusion, Kidney, System And Accessories, Isolated Heart, Transport And Preservation . Use the specialty filter in the sidebar to narrow results.