Cardiologs Technologies is one of 272 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Cardiologs Technologies - FDA 510(k) Cleared Devices
Recent clearances: Cardiologs Holter Platform, CardioLogs ECG Analysis Platform
2
Total
2
Cleared
0
Denied
Cardiologs Technologies has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.
Last cleared in 2021. Active since 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cardiologs Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Daniel & Daniel Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cardiologs Technologies
2 devices