# K063717: CF-1

- Pathway: 510(k) (Traditional)
- Applicant: Canon, Inc.
- Decided: Jan 23, 2007 after 40 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: 2 generations back to K946058 (1995). 2 ancestors in all.
18 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041546: Digital Fundus Camera, Model CF-60DSI, Canon, Inc. (2004) Summary page 1.

## Most influential descendants
- K080883: CR-1 (2008), 17 descendants of its own
- K092565: Digital Retinal Camera CX-1 (2010), 14 descendants of its own
- K112330: Kowa VX-20 (2012), 6 descendants of its own
- K090466: Digital Retinal Camera, CR-1 Mark II (2009), 5 descendants of its own
- K102013: Digital Retinal Camera (2010), 4 descendants of its own

## Indications for use
The device is intended to be used for taking digital images of retina of human eye with a mydriatic.

Source page: https://510kreport.com/device/K063717
Methodology: https://510kreport.com/methodology