Parker Hannifin is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Parker Hannifin - FDA 510(k) Cleared Devices
Recent clearances: Nitronox Plus 0-70, Nitronox 0-50, Nitronox Plus 50/50
1
Total
1
Cleared
0
Denied
Parker Hannifin has 1 FDA 510(k) cleared medical devices. Based in Hatfield, US.
Last cleared in 2021. Active since 2021. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Parker Hannifin Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Parker Hannifin
1 devices