# K001698: Micro Link Endoscopic Fiber Cable, Model B1-90159

- Pathway: 510(k) (Traditional)
- Applicant: Cogent Light Technologies, Inc.
- Decided: Jul 17, 2000 after 45 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.
3 later devices descend from it; 3 cite it directly.
0 of 4 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
- 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
- K063309: Tru-Cable (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K001698
Methodology: https://510kreport.com/methodology