K-number	K912165
Device name	LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEM
Applicant	Menlo Care, Inc.
Product code	FOZ
Device class	Class II
Decision date	Dec 11, 1991
Decision	Substantially Equivalent — Kit Device
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEM

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