# K901035: Fiber Optic Light Guide or Fiber Optic Cable

- Pathway: 510(k) (Traditional)
- Applicant: Cuda Products Co.
- Decided: Apr 23, 1990 after 48 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; 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K200874: TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End (2020), 0 descendants of its own
- K141330: Endo-Cord (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K901035
Methodology: https://510kreport.com/methodology