Aerogen, Ltd.

Aerogen, Ltd. — FDA 510(k) Submissions

Aerogen, Ltd. has submitted 5 FDA 510(k) premarket notifications since 2011, of which 5 received clearance as substantially equivalent to a predicate device.

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