Automatic Liquid Packaging, Inc.

Automatic Liquid Packaging, Inc. — FDA 510(k) Submissions

Automatic Liquid Packaging, Inc. has submitted 21 FDA 510(k) premarket notifications since 1983, of which 21 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nebulizer (direct Patient Interface), Humidifier, Respiratory Gas, (direct Patient Interface), Tube, Tracheostomy (w/wo Connector), Tube Tracheostomy And Tube Cuff, Accessories, Soft Lens Products . Use the specialty filter in the sidebar to narrow results.