# K192404: Patient Monitoring Cable (SpO2 Extension Cable)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Coreray Technology, Ltd.
- Decided: Jun 22, 2020 after 293 days
- Product code: DSA (Cable, Transducer And Electrode, Patient, (Including Connector))
- Device class: 2
- Regulation: 21 CFR 870.2900
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K992524 (2000). 3 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120010: Cable/ Lead-Wire (Ecg, Ekg, SPO2 and Invasive Blood Pressure), Shenzhen Med-Link Electronics Tech Co., Ltd. (2012) Summary page 5.

## Most influential descendants
- K222370: SpO2 Extension Cable (2023), 1 descendant of its own
- K242986: SpO2 Extension Cable (2025), 0 descendants of its own

## Indications for use
Patient Monitoring Cables are intended to be used to connect sensors, placed at appropriate sites on the patient to a monitoring device for general monitoring by health care professional.

Source page: https://510kreport.com/device/K192404
Methodology: https://510kreport.com/methodology