K-number	K230535
Device name	KARL STORZ Urological Laser Accessories
Applicant	Karl Storz SE & CO. KG
Product code	GEX
Device class	Class II
Decision date	Sep 8, 2023
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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KARL STORZ Urological Laser Accessories

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