Aesku.Diagnostics GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Aesku.Diagnostics GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: AESKUSLIDES ANCA Ethanol, AESKUSLIDES ANCA Formalin, AESKUSLIDES nDNA (Crithidia luciliae), AESKUSLIDES nDNA (Crithidia luciliae) Demo Kit, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x5, AESKUSLIDES nDNA (Crithidia luciliae) Bulk kit x10
2
Total
2
Cleared
0
Denied
Aesku.Diagnostics GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Wendeslheim, DE.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Aesku.Diagnostics GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aesku.Diagnostics GmbH & Co. KG
2 devices