K-number	K190312
Device name	Dornier Ureteral Stent
Applicant	Dornier Medtech America, Inc.
Product code	FAD
Device class	Class II
Decision date	Nov 15, 2019
Decision	Substantially Equivalent
Regulation	876.4620

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Source

View the full FDA submission: accessdata.fda.gov

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Dornier Ureteral Stent

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