Medical Device Manufacturer · US , Lake Zurich , IL

Fresenius Kabi USA,Llc - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2016
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: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Fresenius Kabi USA,Llc Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Fresenius Kabi USA,Llc

2 devices
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