Henning Knudsen Engineering A/S is one of 65 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Henning Knudsen Engineering A/S - FDA 510(k) Cleared Devices
Recent clearances: K-SYSTEMS WORK STATIONS, TYPE L-13W, L-13E, L-13ES, L-13ET, L-13EM, L-23, L-23E, L-24, L-24E, L-25, L-25E, L-26, L-26E,L
1
Total
1
Cleared
0
Denied
Henning Knudsen Engineering A/S has 1 FDA 510(k) cleared medical devices. Based in Birkerod, DK.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Henning Knudsen Engineering A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Henning Knudsen Engineering A/S
1 devices