K-number	K771022
Device name	CATHETER, UMBILICAR ARTERY
Applicant	Axiom Medical, Inc.
Product code	FOS
Device class	Class II
Decision date	Nov 29, 1977
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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CATHETER, UMBILICAR ARTERY

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