B?hlmann Laboratories AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
B?hlmann Laboratories AG - FDA 510(k) Cleared Devices
Recent clearances: BÜHLMANN fCAL® turbo and CALEX® Cap
1
Total
1
Cleared
0
Denied
B?hlmann Laboratories AG has 1 FDA 510(k) cleared medical devices. Based in Sch?nenbuch, CH.
Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by B?hlmann Laboratories AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by QUARAS, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - B?hlmann Laboratories AG
1 devices