K-number	K201340
Device name	AQUILA 320 D / AQUILA 320 S
Applicant	Vmi Tecnologias Ltda
Product code	IZL
Device class	Class II
Decision date	Jun 19, 2020
Decision	Substantially Equivalent
Regulation	892.1720

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Source

View the full FDA submission: accessdata.fda.gov

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AQUILA 320 D / AQUILA 320 S

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