K-number	K021941
Device name	SAMPLOK LUER KIT
Applicant	Itl Corporation Pty, Ltd.
Product code	JKA
Device class	Class II
Decision date	Jul 2, 2002
Decision	Substantially Equivalent
Regulation	862.1675

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View the full FDA submission: accessdata.fda.gov

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SAMPLOK LUER KIT

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