Jansson A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Jansson A/S - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Jansson A/S has 1 FDA 510(k) cleared medical devices. Based in Vejle, DK.
Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Jansson A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jansson A/S
1 devices