# K192488: CO2 Sidestream Module

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Kingst Commercial & Trade Co., Ltd.
- Decided: May 22, 2020 after 254 days
- Product code: CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase)
- Device class: 2
- Regulation: 21 CFR 868.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 12 generations back to K962603 (1997). 48 ancestors in all.
No later device cites it as a predicate yet.
1 of 49 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170820: Capnograph and Oximeter, Cmi Health, Inc. (2018) Summary page 5.
- K053174: Loflo C5 CO2 Sensor, Respironics Novametrix, LLC (2006) Summary page 5.

## Indications for use
The CO2 Sidestream Module is designed to provide carbon dioxide monitoring to a host monitoring system during anesthesia / recovery, in the intensive care unit (ICU), and in Respiratory care. The CO2 Sidestream Module is used for adult patients.

Source page: https://510kreport.com/device/K192488
Methodology: https://510kreport.com/methodology