K-number	K043021
Device name	STRYKER URETEROSCOPE
Applicant	Stryker Endoscopy
Product code	FGB
Device class	Class II
Decision date	Mar 16, 2005
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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STRYKER URETEROSCOPE

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