# K252979: Voyager DSLT (430840610)

- Pathway: 510(k) (Traditional)
- Applicant: Belkin Vision, Ltd.
- Decided: Apr 7, 2026 after 202 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: 6 generations back to K894841 (1989). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K230722: Eagle device, Belkin Vision, Ltd. (2023) Summary page 5.

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

Source page: https://510kreport.com/device/K252979
Methodology: https://510kreport.com/methodology