K-number	K900904
Device name	CANDELA DIRECTABLE BILIARY CATHETER SYSTEM
Applicant	Candela Laser Corp.
Product code	FGE
Device class	Class II
Decision date	May 11, 1990
Decision	Substantially Equivalent
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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CANDELA DIRECTABLE BILIARY CATHETER SYSTEM

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