# K090774: Lightlas Selector

- Pathway: 510(k) (Traditional)
- Applicant: Lightmed Corp.
- Decided: Aug 13, 2009 after 143 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: 4 generations back to K894841 (1989). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081704: Selecta Family of Ophithalmic Laser Systems, Lumenis, Inc. (2008) Summary page 1.
- K021550: Lumenis Selecta Duet, Ellex Medical Pty, Ltd. (2002) Summary page 1.

## Indications for use
LightLas Lpulsa SYL-9000: Photodisruption of ocular tissue using light energy emitted by a Nd:YAG laser, including posterior capsulotomy and pupillary membranectomy. LightLas SeLecTor Deux: Photodisruption of ocular tissue using light energy emitted by a Nd:YAG laser, including posterior capsulotomy, pupillary membranectomy and selective laser trabeculoplasty. LightLas LaserLink: Laser delivery system for use by an ophthalmologist in the treatment of ocular tissue. The laser delivery system is intended for a variety of ophthalmic uses, including the indications specified in the laser operator manual. Refer to the laser operator manual, General Intended Use section. LightLas SecLeTor Trois: (SeLecTor Deux with LightLas 532 or 561 or 810) Photodisruption of ocular tissue using light energy emitted by a Nd:YAG laser, including posterior capsulotomy, and pupillary membranectomy, retinal photocoagulation and selective laser trabeculoplasty.

Source page: https://510kreport.com/device/K090774
Methodology: https://510kreport.com/methodology