K-number	K811535
Device name	MODEL FUS-1, FLEXIBLE URETEROSCOPE
Applicant	American Optical Corp.
Product code	FGB
Device class	Class II
Decision date	Jun 23, 1981
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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MODEL FUS-1, FLEXIBLE URETEROSCOPE

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