K-number	K071423
Device name	MEDLINE LATEX FOLEY CATHETER
Applicant	Medline Industries, Inc.
Product code	EZL
Device class	Class II
Decision date	Jul 18, 2007
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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MEDLINE LATEX FOLEY CATHETER

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