K-number	K211347
Device name	Uretero1 Ureteroscope System
Applicant	STERIS Corporation
Product code	FGB
Device class	Class II
Decision date	Nov 23, 2021
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Uretero1 Ureteroscope System

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