K-number	K993904
Device name	INTRASTENT DOUBLESTRUT LD
Applicant	Intratherapeutics, Inc.
Product code	FGE
Device class	Class II
Decision date	Feb 1, 2000
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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INTRASTENT DOUBLESTRUT LD

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