K-number	K221349
Device name	XPER Technology PREMIUM Pro Blood Glucose Monitoring System
Applicant	Taidoc Technology Corporation
Product code	PZI
Device class	Class II
Decision date	Nov 19, 2024
Decision	Substantially Equivalent
Regulation	862.1345

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Source

View the full FDA submission: accessdata.fda.gov

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XPER Technology PREMIUM Pro Blood Glucose Monitoring System

Everything you need for a 510(k) submission. Nothing you don't.