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FDA 510(k)

Nihon Kohden CO2 Monitor

K-Number: K171765 · 2017-10-11

ApplicantNihon Kohden Corporation
Decision Date2017-10-11
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Nihon Kohden CO2 Monitor is a medical device manufactured by Nihon Kohden Corporation. It received FDA 510(k) clearance on 2017-10-11 under approval number K171765. 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 Nihon Kohden CO2 Monitor?

Nihon Kohden CO2 Monitor is a medical device that received FDA 510(k) clearance on 2017-10-11. It is manufactured by Nihon Kohden Corporation. The 510(k) number is K171765.

When was Nihon Kohden CO2 Monitor approved by the FDA?

Nihon Kohden CO2 Monitor received FDA 510(k) clearance on 2017-10-11, under approval number K171765.

What company makes Nihon Kohden CO2 Monitor?

Nihon Kohden CO2 Monitor is manufactured by Nihon Kohden Corporation.

What is the FDA product code for Nihon Kohden CO2 Monitor?

The FDA product code for Nihon Kohden CO2 Monitor is CCK.

Other Devices by Nihon Kohden Corporation

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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 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. K161860TG-970P CO2 Sensor KitNihon Kohden Corporation

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.

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