# K081774: Solx 790 Titanium Sapphire Laser

- Pathway: 510(k) (Traditional)
- Applicant: Solx, Inc.
- Decided: Sep 12, 2008 after 81 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: 1 generation back to K913127 (1991). 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)
- K913127: Coherent Novus 3000 Argon Photocoagulator, Coherent Medical Group (1991) Summary page 1.

## Indications for use
Laser trabeculoplasty to reduce intraocular pressure in patients with poorly controlled intraocular pressure on maximally tolerated medical therapy or prior failed laser trabeculoplasty

Source page: https://510kreport.com/device/K081774
Methodology: https://510kreport.com/methodology