K-number	K113869
Device name	ORIGEN REINFORCED DUAL LUMEN CATHETER
Applicant	Origen Biomedical, Inc.
Product code	DWF
Device class	Class II
Decision date	Jul 26, 2012
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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ORIGEN REINFORCED DUAL LUMEN CATHETER

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