K-number	K923096
Device name	URESIL BILLIARY CATHETER
Applicant	Uresil Corp.
Product code	FGE
Device class	Class II
Decision date	Jul 13, 1993
Decision	Substantially Equivalent
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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URESIL BILLIARY CATHETER

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