Kjaerulff Rehabilitation A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Kjaerulff Rehabilitation A/S - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kjaerulff Rehabilitation A/S has 1 FDA 510(k) cleared medical devices. Based in Otterup, DK.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Kjaerulff Rehabilitation A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kjaerulff Rehabilitation A/S
1 devices