K-number	K180824
Device name	VaPro 2 Intermittent Catheter
Applicant	Hollister Incorporated
Product code	GBM
Device class	Class II
Decision date	Jun 22, 2018
Decision	Substantially Equivalent
Regulation	876.5130

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Source

View the full FDA submission: accessdata.fda.gov

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VaPro 2 Intermittent Catheter

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