K-number	K983867
Device name	FUJI CATHETER, MODEL CTH001
Applicant	Windy Hill Technology, Inc.
Product code	KNW
Device class	Class II
Decision date	Jun 9, 1999
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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FUJI CATHETER, MODEL CTH001

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