Cnsystem Medizintechnik AG is one of 40 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Cnsystem Medizintechnik AG - FDA 510(k) Cleared Devices
Recent clearances: NON-INVASIVE CONTINUOUS BLOOD PRESSURE MONITORING SYSTEM CNAP MONITOR 500I, 500AT
1
Total
1
Cleared
0
Denied
Cnsystem Medizintechnik AG has 1 FDA 510(k) cleared medical devices. Based in Graz, AT.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cnsystem Medizintechnik AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Sud America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cnsystem Medizintechnik AG
1 devices