K-number	K150233
Device name	NIOX VERO Airway Inflammation Monitor
Applicant	Aerocrine AB
Product code	MXA
Device class	Class II
Decision date	Feb 26, 2015
Decision	Substantially Equivalent
Regulation	862.3080

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Source

View the full FDA submission: accessdata.fda.gov

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NIOX VERO Airway Inflammation Monitor

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