Parker Hannifin Corporation

Parker Hannifin Corporation — FDA 510(k) Submissions

Parker Hannifin Corporation has submitted 5 FDA 510(k) premarket notifications since 2016, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powered Exoskeleton, Apparatus, Gas-scavenging, Mixer, Breathing Gases, Anesthesia Inhalation . Use the specialty filter in the sidebar to narrow results.