Medical Device Manufacturer · DE , Wendeslheim

Aesku.Diagnostics GmbH & Co. KG

2 submissions · 2 cleared · Since 2018
2
Total
2
Cleared
0
Denied

Aesku.Diagnostics GmbH & Co. KG — FDA 510(k) Submissions

Aesku.Diagnostics GmbH & Co. KG has submitted 2 FDA 510(k) premarket notifications since 2018, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Anti-dna Antibody, Antigen And Control, Test System, Antineutrophil Cytoplasmic Antibodies (anca) . Use the specialty filter in the sidebar to narrow results.

2 devices
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All2 Immunology 2