Mequ A/S is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Mequ A/S - FDA 510(k) Cleared Devices
Recent clearances: °M Warmer System with °M Station, °M Warmer System
2
Total
2
Cleared
0
Denied
Mequ A/S has 2 FDA 510(k) cleared medical devices. Based in Kobenhavn N, DK.
Latest FDA clearance: Apr 2026. Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Mequ A/S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mequ A/S
2 devices