Diasys Diagnostic Systems GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Diasys Diagnostic Systems GmbH - FDA 510(k) Cleared Devices
Recent clearances: DiaSys Procalcitonin FS
1
Total
1
Cleared
0
Denied
Diasys Diagnostic Systems GmbH has 1 FDA 510(k) cleared medical devices. Based in Holzheim, DE.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Diasys Diagnostic Systems GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Imagenix, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Diasys Diagnostic Systems GmbH
1 devices