Lifescan Europe is one of 79 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Lifescan Europe - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Lifescan Europe has 2 FDA 510(k) cleared medical devices. Based in Zug, CH.
Historical record: 2 cleared submissions from 2015 to 2015. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Lifescan Europe Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lifescan Europe
2 devices