# K120825: Supra Scan Delivery System

- Pathway: 510(k) (Traditional)
- Applicant: Quantel Medical
- Decided: Sep 14, 2012 after 179 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: 8 generations back to K894841 (1989). 29 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100678: Supra Scan Delivery System, Quantel Medical (2010) Summary page 1.
- K111108: Pascal Streamline 577 (with Accessories), Topcon Medical Laser Systems, Inc. (2011)
- K071687: Famili of Iridex IQ Laser Systems, Iridex Corp (2008) Summary page 1.

## Most influential descendants
- K170067: Easyret (2017), 0 descendants of its own

## Indications for use
The SUPRA SCAN Delivery System when connected to a compatible laser system is indicated for use in the treatment of ocular pathology of anterior and posterior segments including, retinal photocoagulation, pan retinal photocoagulation for vascular and structural abnormalities of the retina and choroids including: * Proliferative and nonproliferative diabetic retinopathy; * Choroidal neovascularization; * Branch retinal vein occlusion; * Treatment of choroidal neovascularization associated with wet age-related macular degeneration; * Retinal tears and detachments * Macular edema * Retinopathy of Prematurity * Iridotomy and trabeculoplasty in angle closure glaucoma and open angle glaucoma.

Source page: https://510kreport.com/device/K120825
Methodology: https://510kreport.com/methodology