Parker Hannifin - FDA 510(k) Cleared Devices

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.