Pari Respiratory Equipment, Inc.

Pari Respiratory Equipment, Inc. — FDA 510(k) Submissions

Pari Respiratory Equipment, Inc. has submitted 10 FDA 510(k) premarket notifications since 2009, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nebulizer (direct Patient Interface), Spirometer, Therapeutic (incentive) . Use the specialty filter in the sidebar to narrow results.