Parker Hannifin Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Parker Hannifin Corporation - FDA 510(k) Cleared Devices
Recent clearances: Midas Flowmeter, Nitronox Scavenger Plus, Indego(R)
5
Total
5
Cleared
0
Denied
Parker Hannifin Corporation has 5 FDA 510(k) cleared medical devices. Based in Macedonia, US.
Latest FDA clearance: Sep 2024. Active since 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Parker Hannifin Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Parker Hannifin Corporation
5 devices