Fiegert-Endotech Medizintechnik GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Fiegert-Endotech Medizintechnik GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Fiegert-Endotech Medizintechnik GmbH has 1 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.
Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Fiegert-Endotech Medizintechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fiegert-Endotech Medizintechnik GmbH
1 devices