Gunter Bissinger Medizintechnik GmbH is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Gunter Bissinger Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: Bipolar Micro-Coagulation Forceps
2
Total
2
Cleared
0
Denied
Gunter Bissinger Medizintechnik GmbH has 2 FDA 510(k) cleared medical devices. Based in Amsterdam, Nh, NL.
Historical record: 2 cleared submissions from 2004 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gunter Bissinger Medizintechnik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gunter Bissinger Medizintechnik GmbH
2 devices