# K864387: Luxtec Fiberoptic Cables

- Pathway: 510(k) (Traditional)
- Applicant: Luxtec Corp.
- Decided: May 22, 1987 after 198 days
- Product code: EQH (Source, Carrier, Fiberoptic Light)
- Device class: 1
- Regulation: 21 CFR 874.4350
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Feb 7, 2007 · Not classified · Z-0698-2007: Light Degradation in transmission-A film may deposit on the front face and limit transmission of light

Source page: https://510kreport.com/device/K864387
Methodology: https://510kreport.com/methodology