Hertart is one of 101 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Hertart - FDA 510(k) Cleared Devices
Recent clearances: Micro well group culture dish, 9-well, CULTURE DISH 40 MM, CULTURE DISH 60 MM, MICRO DROPLET CULTURE DISH, 5 WELL CULTURE DISH, CENTRE WELL DISH, ICSI DISH
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.
510(k) submissions have been managed by Hertart Aps as regulatory consultant.
FDA 510(k) Regulatory Record - Hertart
2 devices