Angiomed GmbH & Co. Medizintechnik KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Angiomed GmbH & Co. Medizintechnik KG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Angiomed GmbH & Co. Medizintechnik KG has 1 FDA 510(k) cleared medical devices. Based in Germany, DE.
Historical record: 1 cleared submissions from 1992 to 1992. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Angiomed GmbH & Co. Medizintechnik KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Angiomed GmbH & Co. Medizintechnik KG
1 devices