Puracath Medical, Inc.

Puracath Medical, Inc. — FDA 510(k) Submissions

Puracath Medical, Inc. has submitted 3 FDA 510(k) premarket notifications since 2016, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Set, Administration, Intravascular, Set, Administration, For Peritoneal Dialysis, Disposable . Use the specialty filter in the sidebar to narrow results.