K-number	K150935
Device name	SpeediCath Compact Eve
Applicant	Coloplast A/S
Product code	GBM
Device class	Class II
Decision date	Jul 2, 2015
Decision	Substantially Equivalent
Regulation	876.5130

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Source

View the full FDA submission: accessdata.fda.gov

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SpeediCath Compact Eve

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