K-number	K220090
Device name	Visibly Digital Acuity Product
Applicant	Visibly, Inc.
Product code	QTO
Device class	Class I
Decision date	Aug 12, 2022
Decision	Substantially Equivalent
Regulation	886.1150

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Source

View the full FDA submission: accessdata.fda.gov

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Visibly Digital Acuity Product

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