Airamed GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Airamed GmbH - FDA 510(k) Cleared Devices
Recent clearances: AIRAscore
1
Total
1
Cleared
0
Denied
Airamed GmbH has 1 FDA 510(k) cleared medical devices. Based in T?bingen, DE.
Last cleared in 2023. Active since 2023. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Airamed GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Johner Institut GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Airamed GmbH
1 devices