# K024072: Duckworth & Kent LTD Lens Delivery System

- Pathway: 510(k) (Traditional)
- Applicant: Duckworth & Kent, Ltd.
- Decided: Oct 6, 2003 after 300 days
- Product code: MSS (Folders And Injectors, Intraocular Lens (Iol))
- Device class: 1
- Regulation: 21 CFR 886.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Folding and injection of Chiron Soflex L161U lens implant into the eye using a Chiron Microsert IC-SBU disposable cartridge.

Source page: https://510kreport.com/device/K024072
Methodology: https://510kreport.com/methodology