Safety lancet (XXVIII, XXIX, XXX, XXXI, XXXII, XXXIII, XXXIV.) (K240806) — FDA 510(k) Clearance | Predicase

K-number	K240806
Device name	Safety lancet (XXVIII, XXIX, XXX, XXXI, XXXII, XXXIII, XXXIV.)
Applicant	Tianjin Huahong Technology Co., Ltd.
Product code	FMK
Device class	Class II
Decision date	May 21, 2024
Decision	Substantially Equivalent
Regulation	878.4850

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View the full FDA submission: accessdata.fda.gov

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