Medical Device Manufacturer · SE , Goteborg

Qualisys AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018

Total

Cleared

Denied

Qualisys AB has 1 FDA 510(k) cleared medical devices. Based in Goteborg, SE.

Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Qualisys AB Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Qualisys AB

1 devices

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