K-number	K223354
Device name	EGIS Biliary Single Bare Stent
Applicant	S&G Biotech, Inc.
Product code	FGE
Device class	Class II
Decision date	Sep 21, 2023
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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EGIS Biliary Single Bare Stent

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