K-number	K162109
Device name	Kwart Retro-Inject Ureteral Stent
Applicant	Cook Incorporated
Product code	FAD
Device class	Class II
Decision date	Jun 7, 2017
Decision	Substantially Equivalent
Regulation	876.4620

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View the full FDA submission: accessdata.fda.gov

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Kwart Retro-Inject Ureteral Stent

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