K-number	K172278
Device name	Firlit-Kluge Urethral Stent, Koyle Diaper Stent, Zaontz Urethral Stent
Applicant	Cook Incorporated
Product code	GBM
Device class	Class II
Decision date	Nov 22, 2017
Decision	Substantially Equivalent
Regulation	876.5130

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View the full FDA submission: accessdata.fda.gov

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Firlit-Kluge Urethral Stent, Koyle Diaper Stent, Zaontz Urethral Stent

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