K-number	K093510
Device name	LUMENVU CATHETER GUIDANCE SYSTEM
Applicant	Sonosite,Inc.
Product code	OMF
Device class	Class II
Decision date	Aug 23, 2010
Decision	Substantially Equivalent
Regulation	880.5970

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Source

View the full FDA submission: accessdata.fda.gov

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LUMENVU CATHETER GUIDANCE SYSTEM

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