K-number	K192577
Device name	Actreen Hi-Lite Intermittent Urinary Catheters
Applicant	B.Braun Medical, Inc.
Product code	GBM
Device class	Class II
Decision date	May 7, 2020
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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Actreen Hi-Lite Intermittent Urinary Catheters

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