Gke-GmbH is one of 198 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Gke-GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Gke-GmbH has 1 FDA 510(k) cleared medical devices. Based in Waldems, DE.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Gke-GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gke-GmbH
1 devices