Liquet Medical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Liquet Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Glen Allen, US.
Latest FDA clearance: Feb 2026. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Liquet Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Evergreen Strategic Consulting as regulatory consultant.
2 devices