K-number	K223120
Device name	Ventoux VC2; Ventoux VC3
Applicant	Flight Medical Innovations , Ltd.
Product code	CBK
Device class	Class II
Decision date	Dec 2, 2024
Decision	Substantially Equivalent
Regulation	868.5895

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Source

View the full FDA submission: accessdata.fda.gov

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Ventoux VC2; Ventoux VC3

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