# K113330: Cablecap

- Pathway: 510(k) (Traditional)
- Applicant: Sensormed
- Decided: Jan 12, 2012 after 59 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
Longest line of descent: 4 generations back to K042034 (2004). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101496: Cablecap Model: WLF, STZ, Acm, Sensormed (2010) Summary page 1.

## Indications for use
The device absorbs and diffuses the light transmitted through the cable in order to prevent patient burns and igniting flammable items in the surgical suite.

Source page: https://510kreport.com/device/K113330
Methodology: https://510kreport.com/methodology