King Systems Corp.

King Systems Corp. — FDA 510(k) Submissions

King Systems Corp. has submitted 18 FDA 510(k) premarket notifications since 1988, of which 18 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filter, Bacterial, Breathing-circuit, Airway, Oropharyngeal, Anesthesiology, Circuit, Breathing (w Connector, Adaptor, Y Piece), Device, Fixation, Tracheal Tube, Absorber, Carbon-dioxide . Use the specialty filter in the sidebar to narrow results.