K-number	K190032
Device name	Disposable Sclerotherapy Needle
Applicant	Hangzhou AGS MedTech Co., Ltd.
Product code	FBK
Device class	Class II
Decision date	Feb 27, 2020
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Disposable Sclerotherapy Needle

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