Qynapse is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Qynapse - FDA 510(k) Cleared Devices
Recent clearances: QyScore Software
1
Total
1
Cleared
0
Denied
Qynapse has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Qynapse 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 - Qynapse
1 devices