K-number	K830372
Device name	ARTIMICROBIAL REMOVAL DEVICE
Applicant	Marion Laboratories, Inc.
Product code	LJF
Device class	Class I
Decision date	Apr 8, 1983
Decision	Substantially Equivalent
Regulation	866.2560

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View the full FDA submission: accessdata.fda.gov

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ARTIMICROBIAL REMOVAL DEVICE

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