Medical Device Manufacturer · US , Windham , NH

Buhlmann Laboratories AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1995

Total

Cleared

Denied

Buhlmann Laboratories AG has 4 FDA 510(k) cleared medical devices. Based in Windham, US.

Historical record: 4 cleared submissions from 1995 to 2019. Primary specialty: Immunology.

Browse the FDA 510(k) cleared devices submitted by Buhlmann Laboratories AG Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Buhlmann Laboratories AG

4 devices

1-4 of 4