K-number	K233418
Device name	Biofourmis Everion+ (G2)
Applicant	Biofourmis Singapore Pte., Ltd.
Product code	MSX
Device class	Class II
Decision date	May 9, 2024
Decision	Substantially Equivalent
Regulation	870.2300

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View the full FDA submission: accessdata.fda.gov

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Biofourmis Everion+ (G2)

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