Fresenius Kabi USA,Llc is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fresenius Kabi USA,Llc - FDA 510(k) Cleared Devices
Recent clearances: AMICUS Separator System, AMICUS Exchange Kit - Therapeutics, Waste Transfer Set, Blood Component Filter Set With Vented Spike and Luer Adapter
2
Total
2
Cleared
0
Denied
Fresenius Kabi USA,Llc has 2 FDA 510(k) cleared medical devices. Based in Lake Zurich, US.
Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Fresenius Kabi USA,Llc Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Fresenius Kabi USA,Llc
2 devices