K-number	K221419
Device name	TD-5010 Lancing Device and TD-5084 Sterile Lancets
Applicant	Gostar Co., Ltd.
Product code	QRL
Device class	Class II
Decision date	Jan 20, 2023
Decision	Substantially Equivalent
Regulation	878.4850

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View the full FDA submission: accessdata.fda.gov

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TD-5010 Lancing Device and TD-5084 Sterile Lancets

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