Kline Europe GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kline Europe GmbH has 1 FDA 510(k) cleared medical devices. Based in Dusseldorf, DE.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Kline Europe GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Kline Europe GmbH
1 devices