K-number	K041826
Device name	EKOS ULTRASOUND INFUSION SYSTEM
Applicant	Ekos Corp.
Product code	NUI
Device class	Class II
Decision date	Apr 27, 2005
Decision	Unknown
Regulation	870.1200

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Source

View the full FDA submission: accessdata.fda.gov

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EKOS ULTRASOUND INFUSION SYSTEM

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