# K072912: Sopro 225 Dual Halogen Light Source

- Pathway: 510(k) (Traditional)
- Applicant: Sopro
- Decided: Nov 16, 2007 after 35 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- 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 K010033 (2002). 1 ancestor in all.
10 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010033: Light Projector with Endoscopic Camera, 1 CCD Camera Head NTSC, 1 CCD Camera Head Pal, Light Projector, Model 5551.107, Richard Wolf Medical Instruments Corp. (2002) Summary page 1.

## Most influential descendants
- K091829: PLS Portable Light Source (2009), 9 descendants of its own
- K130503: Pathassist Led Light Fiber (2013), 6 descendants of its own
- K141916: Pathassist Led Light Fiber (2014), 5 descendants of its own
- K152435: PassAssist LED Light Fiber (2015), 2 descendants of its own
- K212774: VenSure LightGuide (2022), 1 descendant of its own

## Indications for use
Provides light for examination, diagnostic and therapeutic applications, particularly in endoscopy

Source page: https://510kreport.com/device/K072912
Methodology: https://510kreport.com/methodology