K-number	K110202
Device name	FUJIFILM DIAGNOSTIC ULTRASOUND SYSTEM FAZONE CB
Applicant	Fujifilm Medical System U.S.A., Inc.
Product code	ITX
Device class	Class II
Decision date	Feb 8, 2011
Decision	Substantially Equivalent
Regulation	892.1570

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View the full FDA submission: accessdata.fda.gov

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FUJIFILM DIAGNOSTIC ULTRASOUND SYSTEM FAZONE CB

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