Lifescan Europe is one of 118 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Lifescan Europe - FDA 510(k) Cleared Devices
Recent clearances: OneTouch Ultra Plus Flex Blood Glucose Monitoring System, OneTouch Verio Flex Blood Glucose Monitoring System
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.
510(k) submissions have been managed by Lifescan Scotland, Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Lifescan Europe
2 devices