K-number	K010349
Device name	DUAL LUMEN MIDLINE CATHETER
Applicant	Catheter Innovations, Inc.
Product code	LJS
Device class	Class II
Decision date	Feb 28, 2001
Decision	Substantially Equivalent
Regulation	880.5970

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View the full FDA submission: accessdata.fda.gov

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DUAL LUMEN MIDLINE CATHETER

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