Hertart is one of 43 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Hertart - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Hertart has 2 FDA 510(k) cleared medical devices. Based in Greve, DK.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Hertart Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hertart
2 devices