K-number	K232370
Device name	Percutaneous Nephroscope System
Applicant	Karl Storz SE & CO. KG
Product code	FGA
Device class	Class II
Decision date	May 1, 2024
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Percutaneous Nephroscope System

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