Paragonix Technologies, Inc.

Paragonix Technologies, Inc. — FDA 510(k) Submissions

Paragonix Technologies, Inc. has submitted 7 FDA 510(k) premarket notifications since 2013, of which 5 received clearance as substantially equivalent to a predicate device.

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