K-number	K131491
Device name	KITAZATO IUI CATHETER
Applicant	Kitazato Medical Co., Ltd.
Product code	MQF
Device class	Class II
Decision date	Sep 11, 2013
Decision	Substantially Equivalent
Regulation	884.6110

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Source

View the full FDA submission: accessdata.fda.gov

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KITAZATO IUI CATHETER

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