Medical Device Manufacturer · US , Bristol , WI

W.A. Rubbermate Co., Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1997

Total

Cleared

Denied

W.A. Rubbermate Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Bristol, US.

Latest FDA clearance: Feb 2024. Active since 1997. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by W.A. Rubbermate Co., Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by W.A. Rubbermate Co., Ltd.

4 devices

1-4 of 4