Lifescan Europe, A Division of Cilag GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lifescan Europe, A Division of Cilag GmbH has 1 FDA 510(k) cleared medical devices. Based in Zug, CH.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Lifescan Europe, A Division of Cilag GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lifescan Europe, A Division of Cilag GmbH
1 devices