Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50
Apr 2021
237d
Parker Hannifin
1
Total
1
Cleared
0
Denied
Parker Hannifin — FDA 510(k) Submissions
Parker Hannifin has submitted 1 FDA 510(k) premarket notifications since 2021, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Mixer, Breathing Gases, Anesthesia Inhalation . Use the specialty filter in the sidebar to narrow results.
1 devices