CO2 Mainstream Module
K-Number: K192446 · 2020-05-21
Decision Date2020-05-21
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
CO2 Mainstream Module is a medical device manufactured by Beijing Kingst Commercial & Trade Co., Ltd.. It received FDA 510(k) clearance on 2020-05-21 under approval number K192446. 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 Mainstream Module?
CO2 Mainstream Module is a medical device that received FDA 510(k) clearance on 2020-05-21. It is manufactured by Beijing Kingst Commercial & Trade Co., Ltd.. The 510(k) number is K192446.
When was CO2 Mainstream Module approved by the FDA?
CO2 Mainstream Module received FDA 510(k) clearance on 2020-05-21, under approval number K192446.
What company makes CO2 Mainstream Module?
CO2 Mainstream Module is manufactured by Beijing Kingst Commercial & Trade Co., Ltd..
What is the FDA product code for CO2 Mainstream Module?
The FDA product code for CO2 Mainstream Module is CCK.
Other Devices by Beijing Kingst Commercial & Trade Co., Ltd.
Related Devices (Code: CCK)
K162343Westmed Gas Sampling Cannula with O2 deliveryWestmed, Inc.
K151421Nasal CO2 Sample Line, Oral Nasal CO2 Sampling Cannula, O2 Oral/Nasal Co2 Cannula, Sample LinesSalter Labs
K172904IntelliVue Capnography Extension, IntelliVue Microstream ExtensionPhilips Medizin Systeme Boeblingen GmbH
K171765Nihon Kohden CO2 MonitorNihon Kohden Corporation
K171028CARESCAPE Respiratory MOdules, E-sCO, E-sCOV, E-sCOVX, E-sCAiO, E-sCAiOV, E-sCAiOVX and accessoriesGE Healthcare Finland Oy
K161250OC-FLEX Flexible IntraOral CannulaVenture Therapeutics, Inc.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.