Fresenius Pharma is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fresenius Pharma - FDA 510(k) Cleared Devices
3
Total
2
Cleared
0
Denied
Fresenius Pharma has 2 FDA 510(k) cleared medical devices. Based in New Brunswick, US.
Historical record: 2 cleared submissions from 1990 to 1992. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Fresenius Pharma Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fresenius Pharma
3 devices