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.

Qualisys AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Qualisys AB

1 devices

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