K-Systems, Kivex Biotec , Ltd. is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
K-Systems, Kivex Biotec , Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
K-Systems, Kivex Biotec , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Birkerod, DK.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by K-Systems, Kivex Biotec , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - K-Systems, Kivex Biotec , Ltd.
1 devices