K-number	K171765
Device name	Nihon Kohden CO2 Monitor
Applicant	Nihon Kohden Corporation
Product code	CCK
Device class	Class II
Decision date	Oct 11, 2017
Decision	Substantially Equivalent
Regulation	868.1400

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Source

View the full FDA submission: accessdata.fda.gov

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Nihon Kohden CO2 Monitor

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