Cnsystems Medizintechnik GmbH is one of 41 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Cnsystems Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: Task Force CORE, CNAP Monitor, TASK FORCE MONITOR 3040
3
Total
3
Cleared
0
Denied
Cnsystems Medizintechnik GmbH has 3 FDA 510(k) cleared medical devices. Based in Europe, AT.
Last cleared in 2023. Active since 2002. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cnsystems Medizintechnik GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cnsystems Medizintechnik GmbH
3 devices