Duckworth & Kent, Ltd.
Duckworth & Kent, Ltd. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2008.
Top product codes for Duckworth & Kent, Ltd.
Recent clearances by Duckworth & Kent, Ltd.
- K081382 — DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786
- K072985 — DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2
- K060995 — DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788
- K053176 — DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797
- K042478 — CAPSULE TENSION RING INSERTER, MODEL 7-810
- K024072 — DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.