K-number	K181971
Device name	Bander Ureteral Diversion Stent Set, Dretler Ureteroscopy Stent Set
Applicant	Cook Incorporated
Product code	FAD
Device class	Class II
Decision date	Apr 23, 2019
Decision	Unknown
Regulation	876.4620

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Source

View the full FDA submission: accessdata.fda.gov

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Bander Ureteral Diversion Stent Set, Dretler Ureteroscopy Stent Set

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