Medical Device Manufacturer · DK , Hellerup

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

1 submissions · 0 cleared · Since 2020

Total

Cleared

Denied

Acarix A/S has 0 FDA 510(k) cleared medical devices. Based in Hellerup, DK.

Active since 2020. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Acarix A/S Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Acarix A/S

1 devices

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