K-number	K212886
Device name	Broncoflex Agile, Broncoflex Vortex, Screeni
Applicant	Axess Vision Technology
Product code	EOQ
Device class	Class II
Decision date	Feb 16, 2022
Decision	Substantially Equivalent
Regulation	874.4680

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View the full FDA submission: accessdata.fda.gov

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Broncoflex Agile, Broncoflex Vortex, Screeni

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