K-number	K231303
Device name	Arm-type Fully Automatic Digital Blood Pressure Monitor
Applicant	Joytech Healthcare Co. , Ltd.
Product code	DXN
Device class	Class II
Decision date	Jan 26, 2024
Decision	Substantially Equivalent
Regulation	870.1130

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View the full FDA submission: accessdata.fda.gov

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Arm-type Fully Automatic Digital Blood Pressure Monitor

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