Lifescan Europe GmbH is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Lifescan Europe GmbH - FDA 510(k) Cleared Devices
Recent clearances: OneTouch Verio Reflect Blood Glucose Monitoring System
1
Total
1
Cleared
0
Denied
Lifescan Europe GmbH has 1 FDA 510(k) cleared medical devices. Based in Zug, CH.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Lifescan Europe GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lifescan Scotland, Ltd. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Lifescan Europe GmbH
1 devices