K-number	K213186
Device name	NovoFlow Reinforced Ureteral Stent
Applicant	Coloplast Corp.
Product code	FAD
Device class	Class II
Decision date	Feb 16, 2022
Decision	Unknown
Regulation	876.4620

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Source

View the full FDA submission: accessdata.fda.gov

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NovoFlow Reinforced Ureteral Stent

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