# K972225: Ufr Fiberoptic Cable

- Pathway: 510(k) (Traditional)
- Applicant: Universal Fiberoptic Repair, Inc.
- Decided: Mar 18, 1998 after 278 days
- Product code: FST (Light, Surgical, Fiberoptic)
- Device class: 2
- Regulation: 21 CFR 878.4580
- 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; 1 cites 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K023633: Sovis Optique's Endoscopic Cable (2002), 1 descendant of its own
- K063309: Tru-Cable (2007), 0 descendants of its own

## Indications for use
The UFR fiberoptic cable is intended to transmit light for lllumination purposes from light source to various instruments such as headlights, microscopes, gndoscopes. et It 1s manufactured to the buyers' specifications and is intended for use with the buyers’ existing equipment.

Source page: https://510kreport.com/device/K972225
Methodology: https://510kreport.com/methodology