K-number	K071134
Device name	SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM
Applicant	Sonosite,Inc.
Product code	IYO
Device class	Class II
Decision date	May 8, 2007
Decision	Substantially Equivalent
Regulation	892.1560

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View the full FDA submission: accessdata.fda.gov

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SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM

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