K-number	K073596
Device name	NEOMED SINGLE LUMEN UMBILICAL CATHETER
Applicant	Neomed, Inc.
Product code	FOS
Device class	Class II
Decision date	Feb 22, 2008
Decision	Substantially Equivalent
Regulation	880.5200

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Source

View the full FDA submission: accessdata.fda.gov

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NEOMED SINGLE LUMEN UMBILICAL CATHETER

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