# K242061: Reusable Interface Cable 1.5 m (PRD-IFC-002)

- Pathway: 510(k) (Special)
- Applicant: Creo Medical, Ltd.
- Decided: Aug 15, 2024 after 31 days
- Product code: KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories))
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K230328 (2023). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K230328: Speedboat Flush SB1 Instrument, Creo Medical, Ltd. (2023) Summary page 5.

## Indications for use
The Interface Cable is for connection only of a compatible Creo Medical Instrument (Surgical Accessory) to the CROMA Electrosurgical Generator to deliver Radiofrequency (RF) and/or Microwave energy for the cutting, coagulation and ablation of gastrointestinal tissue.

Source page: https://510kreport.com/device/K242061
Methodology: https://510kreport.com/methodology