Airlife, Inc.

Airlife, Inc. — FDA 510(k) Submissions

Airlife, Inc. has submitted 76 FDA 510(k) premarket notifications since 1979, of which 76 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nebulizer (direct Patient Interface), Connector, Airway (extension), Tubing, Pressure And Accessories, Mask, Oxygen, Set, Tubing And Support, Ventilator (w Harness) . Use the specialty filter in the sidebar to narrow results.