Medical Device Manufacturer · DK , Kobenhavn N

Mequ A/S - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024

Total

Cleared

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

1-2 of 2