Slk Medical GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Slk Medical GmbH - FDA 510(k) Cleared Devices
Recent clearances: V12 PRO, VariLymph 12 pro
2
Total
2
Cleared
0
Denied
Slk Medical GmbH has 2 FDA 510(k) cleared medical devices. Based in Dortmund, DE.
Last cleared in 2021. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Slk Medical GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Slk Medical GmbH
2 devices