Medical Device Manufacturer · US , Chester , NY

Biosys AB (Publ) - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Biosys AB (Publ) has 2 FDA 510(k) cleared medical devices. Based in Chester, US.

Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: Neurology.

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

Biosys AB (Publ) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Biosys AB (Publ)

2 devices

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