Medical Device Manufacturer · US , Beaverton , OR

White River (Tm) - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1987

Total

Cleared

Denied

White River (Tm) has 2 FDA 510(k) cleared medical devices. Based in Beaverton, US.

Historical record: 2 cleared submissions from 1987 to 1994. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by White River (Tm) Filter by specialty or product code using the sidebar.

White River (Tm) 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 - White River (Tm)

2 devices

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