Medical Device Manufacturer · US , Frederick , MD

Wieslab AB - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1998

Total

Cleared

Denied

Wieslab AB has 5 FDA 510(k) cleared medical devices. Based in Frederick, US.

Historical record: 5 cleared submissions from 1998 to 1998. Primary specialty: Immunology.

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

Wieslab AB 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 - Wieslab AB

5 devices

1-5 of 5