K-number	K162104
Device name	C-Flex Ureteral Stent Set
Applicant	Cook Incorporated
Product code	FAD
Device class	Class II
Decision date	Apr 24, 2017
Decision	Unknown
Regulation	876.4620

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Source

View the full FDA submission: accessdata.fda.gov

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C-Flex Ureteral Stent Set

Everything you need for a 510(k) submission. Nothing you don't.