K-number	K082815
Device name	WELL LEAD SILICONE AND LATEX FOLEY CATHETERS
Applicant	Well Lead Medical Instruments
Product code	EZL
Device class	Class II
Decision date	Oct 8, 2008
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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WELL LEAD SILICONE AND LATEX FOLEY CATHETERS

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