Medical Device Manufacturer · GB , Hythe, Kent

Sims Portex , Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2000

Total

Cleared

Denied

Sims Portex , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Hythe, Kent, GB.

Historical record: 4 cleared submissions from 2000 to 2002. Primary specialty: Obstetrics & Gynecology.

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

Sims Portex , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sims Portex , Ltd.

4 devices

1-4 of 4