K-number	K092318
Device name	BAXJECT II HI-FLOW NEEDLELESS TRANSFER DEVICE
Applicant	Baxter Healthcare Corporation
Product code	LHI
Device class	Class II
Decision date	Oct 30, 2009
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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BAXJECT II HI-FLOW NEEDLELESS TRANSFER DEVICE

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