K-number	K170422
Device name	BIOSOFT DUO DOUBLE LOOP URETERAL STENTS
Applicant	Coloplast Corp.
Product code	FAD
Device class	Class II
Decision date	Nov 2, 2017
Decision	Substantially Equivalent
Regulation	876.4620

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Source

View the full FDA submission: accessdata.fda.gov

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BIOSOFT DUO DOUBLE LOOP URETERAL STENTS

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