K-number	K890685
Device name	BARD UMBILICAL VESSEL CATHETER
Applicant	C.R. Bard, Inc.
Product code	FOS
Device class	Class II
Decision date	Feb 28, 1989
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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BARD UMBILICAL VESSEL CATHETER

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