Hertart Aps is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Hertart Aps - FDA 510(k) Cleared Devices
Recent clearances: Pasteur Pipette 3mL, Pasteur Pipette 1mL
1
Total
1
Cleared
0
Denied
Hertart Aps has 1 FDA 510(k) cleared medical devices. Based in V?stra Fr?lunda, SE.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Hertart Aps Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hertart Aps
1 devices