Buhlmann Laboratories AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Buhlmann Laboratories AG - FDA 510(k) Cleared Devices
Recent clearances: Buhlmann fCAL turbo and CALEX Cap, BUHLMANN fCAL turbo, BUHLMANN fCAL ELISA
4
Total
4
Cleared
0
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.
Regulatory submissions have been managed by QUARAS, LLC and Mapi Srs, an Icon Plc Company.
FDA 510(k) Regulatory Record - Buhlmann Laboratories AG
4 devices