Dehas Medical Systems GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Dehas Medical Systems GmbH - FDA 510(k) Cleared Devices
Recent clearances: QualityFlow O2 Series (QualityFLOW O2), Quality Mix Blender, Oxymixer
2
Total
2
Cleared
0
Denied
Dehas Medical Systems GmbH has 2 FDA 510(k) cleared medical devices. Based in Luebeck, DE.
Latest FDA clearance: Oct 2024. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Dehas Medical Systems GmbH Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Draeger Medical Systems GmbH and Draeger Medical Systems, Inc..
FDA 510(k) Regulatory Record - Dehas Medical Systems GmbH
2 devices