Hexacath - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Hexacath has 1 FDA 510(k) cleared medical devices. Based in Rueil Malmaison, FR.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Hexacath Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hexacath
1 devices