K-number	K001648
Device name	INTRASTENT DOUBLESTRUT PARAMOUNT
Applicant	Intratherapeutics, Inc.
Product code	FGE
Device class	Class II
Decision date	Aug 28, 2000
Decision	Substantially Equivalent
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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INTRASTENT DOUBLESTRUT PARAMOUNT

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