K-number	K011793
Device name	KSEA FIBERSCOPE
Applicant	KARL STORZ Endoscopy-America, Inc.
Product code	LYK
Device class	Class II
Decision date	Apr 17, 2002
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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KSEA FIBERSCOPE

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