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FDA 510(k)

CO2 Sidestream Module

K-Number: K192488 · 2020-05-22

Decision Date2020-05-22
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CO2 Sidestream Module is a medical device manufactured by Beijing Kingst Commercial & Trade Co., Ltd.. It received FDA 510(k) clearance on 2020-05-22 under approval number K192488. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO2 Sidestream Module?

CO2 Sidestream Module is a medical device that received FDA 510(k) clearance on 2020-05-22. It is manufactured by Beijing Kingst Commercial & Trade Co., Ltd.. The 510(k) number is K192488.

When was CO2 Sidestream Module approved by the FDA?

CO2 Sidestream Module received FDA 510(k) clearance on 2020-05-22, under approval number K192488.

What company makes CO2 Sidestream Module?

CO2 Sidestream Module is manufactured by Beijing Kingst Commercial & Trade Co., Ltd..

What is the FDA product code for CO2 Sidestream Module?

The FDA product code for CO2 Sidestream Module is CCK.

Other Devices by Beijing Kingst Commercial & Trade Co., Ltd.

Related Devices (Code: CCK)

Official Source

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