# K140450: Keeler Kapture Software

- Pathway: 510(k) (Traditional)
- Applicant: Keeler Limited
- Decided: Jun 17, 2014 after 113 days
- Product code: HKI (Camera, Ophthalmic, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K000368 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K000368: Eyecap Imaging System, Clement Clarke Intl., Ltd. (2000) Summary page 1.

## Indications for use
The Keeler Kapture Software Package is used by Health Professionals to capture, store and manage output iniages from Retinal Cameras. Fundus Cameras and Video Slit Lamps

Source page: https://510kreport.com/device/K140450
Methodology: https://510kreport.com/methodology