K-number	K082098
Device name	SONOSITE MAXX SERIES ULTRASOUND SYSTEM
Applicant	Sonosite,Inc.
Product code	IYN
Device class	Class II
Decision date	Aug 25, 2008
Decision	Substantially Equivalent
Regulation	892.1550

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View the full FDA submission: accessdata.fda.gov

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SONOSITE MAXX SERIES ULTRASOUND SYSTEM

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