Medical Device Manufacturer · GB , Runcorn, Cheshire

Steripak, Ltd. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1998

Total

Cleared

Denied

Steripak, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Runcorn, Cheshire, GB.

Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Steripak, Ltd.

2 devices

1-2 of 2