K-number	K081515
Device name	NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0
Applicant	Neomed, Inc.
Product code	FOS
Device class	Class II
Decision date	Jul 21, 2008
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0

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