K-number	K991069
Device name	KSEA NEURO-FIBERSCOPE
Applicant	KARL STORZ Endoscopy-America, Inc.
Product code	GWG
Device class	Class II
Decision date	Jun 3, 1999
Decision	Substantially Equivalent
Regulation	882.1480

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View the full FDA submission: accessdata.fda.gov

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KSEA NEURO-FIBERSCOPE

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