Medical Device Manufacturer · NL , Amsterdam, Nh

Gunter Bissinger Medizintechnik GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Total

Cleared

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: Obstetrics & Gynecology.

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

1-2 of 2