Sanpoint AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Sanpoint AB - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sanpoint AB has 1 FDA 510(k) cleared medical devices. Based in Mariefred, SE.
Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Sanpoint AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sanpoint AB
1 devices