Safety Lancet (XXXV) (K241627) — FDA 510(k) Clearance | Predicase

K-number	K241627
Device name	Safety Lancet (XXXV)
Applicant	Tianjin Huahong Technology Co., Ltd.
Product code	FMK
Device class	Class II
Decision date	Jun 20, 2024
Decision	Substantially Equivalent
Regulation	878.4850

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Source

View the full FDA submission: accessdata.fda.gov

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