Yukon Medical is one of 19020 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Yukon Medical - FDA 510(k) Cleared Devices
Recent clearances: Arisure Closed Vial Adapter, Arisure Dry Spike, Closed Male Luer
3
Total
3
Cleared
0
Denied
Yukon Medical has 3 FDA 510(k) cleared medical devices. Based in Durham, US.
Historical record: 3 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Yukon Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Yukon Medical
3 devices