K-number	K141642
Device name	VAPRO INTERMITTENT CATHETER
Applicant	Hollister Incorporated
Product code	GBM
Device class	Class II
Decision date	Aug 22, 2014
Decision	Substantially Equivalent
Regulation	876.5130

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Source

View the full FDA submission: accessdata.fda.gov

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VAPRO INTERMITTENT CATHETER

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