K-number	K090262
Device name	PERCUCATH URINARY CATHETER
Applicant	Percuvision, LLC
Product code	EZL
Device class	Class II
Decision date	May 28, 2009
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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PERCUCATH URINARY CATHETER

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