# K983714: Solartec Source 270, Model # 90123

- Pathway: 510(k) (Traditional)
- Applicant: Cogent Light Technologies, Inc.
- Decided: Dec 23, 1998 after 63 days
- Product code: FFS (Image, Illumination, Fiberoptic, For Endoscope )
- 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
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K061622: PS Series (2007), 0 descendants of its own
- K070287: PS Series with Fiber Light Guide and Headlight, Models PS200, PS250, PS500 (2007), 0 descendants of its own

## Indications for use
The SolarTec™ Source 270 System is intended for use: 1. To provide visible light for with various rigid or flexible endoscopes, other lighted tools, and surgical headlights that contain fiber bundles or single fibers for illumination 2. In providing illumination for the purposes of allowing observation and manipulation of body cavities and tissues, hollow organs, and canals. 3. With applications that include, but are not limited to, headlights and/or externally illuminated endoscopes used in arthroscopy, bronchoscopy, gynecology, laparoscopy, obstetrics, oto-rhyno-laryngoscopy, urology, and vascular endoscopy as well as surgical headlights used in various open surgical procedures.

Source page: https://510kreport.com/device/K983714
Methodology: https://510kreport.com/methodology