Polamedco, Inc.

Polamedco, Inc. — FDA 510(k) Submissions

Polamedco, Inc. has submitted 20 FDA 510(k) premarket notifications since 1978, of which 20 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tube, Tracheal (w/wo Connector), Connector, Airway (extension), Airway, Nasopharyngeal, Stylet, Tracheal Tube, Tube, Tracheostomy (w/wo Connector) . Use the specialty filter in the sidebar to narrow results.