Medical Device Manufacturer · DK , Kobenhavn N

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

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Mequ A/S has 1 FDA 510(k) cleared medical devices. Based in Kobenhavn N, DK.

Latest FDA clearance: May 2024. 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) cleared devices by Mequ A/S

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