Apoqlar GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Apoqlar GmbH - FDA 510(k) Cleared Devices
Recent clearances: VSI HoloMedicine
1
Total
1
Cleared
0
Denied
Apoqlar GmbH has 1 FDA 510(k) cleared medical devices. Based in Hamburg, DE.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Apoqlar GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Apoqlar GmbH
1 devices