K-number	K993052
Device name	VYGON 2 FR EPICUTANEO PUR-CATHETER
Applicant	Vygon Corp.
Product code	LJS
Device class	Class II
Decision date	Aug 3, 2000
Decision	Substantially Equivalent
Regulation	880.5970

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View the full FDA submission: accessdata.fda.gov

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VYGON 2 FR EPICUTANEO PUR-CATHETER

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