K-number	K241750
Device name	Medifun Safety Lancet ( MSL1 series)
Applicant	Medifun Corporation
Product code	FMK
Device class	Class II
Decision date	Aug 15, 2024
Decision	Substantially Equivalent
Regulation	878.4850

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Source

View the full FDA submission: accessdata.fda.gov

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Medifun Safety Lancet ( MSL1 series)

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