K-number	K091213
Device name	FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMEN
Applicant	Footprint Medical
Product code	FOS
Device class	Class II
Decision date	Sep 25, 2009
Decision	Substantially Equivalent
Regulation	880.5200

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Source

View the full FDA submission: accessdata.fda.gov

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FOOTPRINT MEDICAL UMBILICAL CATHETER, DUAL LUMEN

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