Medical Device Manufacturer · US , Minneapolis, , MN

Beampoint AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Total

Cleared

Denied

Beampoint AB has 1 FDA 510(k) cleared medical devices. Based in Minneapolis,, US.

Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Gastroenterology & Urology.

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

Beampoint 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 - Beampoint AB

1 devices

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