K-number	K032885
Device name	VIDAPORT INTRAOSSEOUS INFUSION SYSTEM
Applicant	Vidacare Corporation
Product code	FMI
Device class	Class II
Decision date	Mar 10, 2004
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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VIDAPORT INTRAOSSEOUS INFUSION SYSTEM

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