Corindus, Inc.

Corindus, Inc. — FDA 510(k) Submissions

Corindus, Inc. has submitted 9 FDA 510(k) premarket notifications since 2012, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Catheter Control, Steerable . Use the specialty filter in the sidebar to narrow results.