K-number	K202747
Device name	Klarity Bolus
Applicant	Klarity Medical & Equipment (GZ) Co., Ltd.
Product code	IYE
Device class	Class II
Decision date	May 14, 2021
Decision	Substantially Equivalent
Regulation	892.5050

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Source

View the full FDA submission: accessdata.fda.gov

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Klarity Bolus

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