Passy-Muir, Inc.

Passy-Muir, Inc. — FDA 510(k) Submissions

Passy-Muir, Inc. has submitted 5 FDA 510(k) premarket notifications since 1995, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tube Tracheostomy And Tube Cuff, Filter, Bacterial, Breathing-circuit . Use the specialty filter in the sidebar to narrow results.