K-number	K222006
Device name	Sclerotherapy & Endoscopic Needles
Applicant	G-Flex Europe Sprl
Product code	FBK
Device class	Class II
Decision date	Apr 3, 2023
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Sclerotherapy & Endoscopic Needles

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