K-number	K091386
Device name	MICROFUSE DUAL RATE INFUSER
Applicant	Numia Medical Technology, LLC
Product code	FRN
Device class	Class II
Decision date	Oct 2, 2009
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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MICROFUSE DUAL RATE INFUSER

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