Medical Device Manufacturer · GB , Baldock, Hertfordshire

Duckworth & Kent, Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2003

Total

Cleared

Denied

Duckworth & Kent, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Baldock, Hertfordshire, GB.

Historical record: 6 cleared submissions from 2003 to 2008. Primary specialty: Ophthalmic.

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

Duckworth & Kent, 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 - Duckworth & Kent, Ltd.

6 devices

1-6 of 6