K-number	K232912
Device name	Facet Aurora Reusable Lancet Base
Applicant	Facet Technologies, LLC
Product code	QRL
Device class	Class II
Decision date	Jan 25, 2024
Decision	Substantially Equivalent
Regulation	878.4850

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Source

View the full FDA submission: accessdata.fda.gov

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Facet Aurora Reusable Lancet Base

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