Pulmonx Corporation

Pulmonx Corporation — FDA 510(k) Submissions

Pulmonx Corporation has submitted 4 FDA 510(k) premarket notifications since 2018, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tube, Tracheal/bronchial, Differential Ventilation (w/wo Connector), Spirometer, Diagnostic, System, X-ray, Tomography, Computed . Use the specialty filter in the sidebar to narrow results.