K-number	K900263
Device name	ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER
Applicant	Arrow Intl., Inc.
Product code	FOZ
Device class	Class II
Decision date	Jul 24, 1990
Decision	Unknown
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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ANTIMICROBIAL MULTI-LUMEN CENTRAL VENOUS CATHETER

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