Rosen Kilde Stenhoj is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rosen Kilde Stenhoj - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Rosen Kilde Stenhoj has 1 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 1 cleared submissions from 1982 to 1982. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Rosen Kilde Stenhoj Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rosen Kilde Stenhoj
1 devices