K-number	K052059
Device name	IUI CATHETER, MODEL 9057
Applicant	Inntec, Inc.
Product code	MQF
Device class	Class II
Decision date	Nov 22, 2005
Decision	Substantially Equivalent
Regulation	884.6110

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View the full FDA submission: accessdata.fda.gov

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IUI CATHETER, MODEL 9057

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