# K230722: Eagle device

- Pathway: 510(k) (Traditional)
- Applicant: Belkin Vision, Ltd.
- Decided: Dec 8, 2023 after 267 days
- Product code: HQF (Laser, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 886.4390
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K894841 (1989). 15 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220877: Selecta Duet LED, Digital Duet, Selecta LED Trio, Digital Trio Laser Systems, Lumenis Be, Inc. (2022) Summary page 5.

## Most influential descendants
- K252979: Voyager DSLT (430840610) (2026), 0 descendants of its own

## Indications for use
The Eagle device is indicated for use in selective laser trabeculoplasty (SLT).

Source page: https://510kreport.com/device/K230722
Methodology: https://510kreport.com/methodology