K-number	K121035
Device name	FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EB-530US
Applicant	Fujifilm Medical System U.S.A., Inc.
Product code	EOQ
Device class	Class II
Decision date	Jun 4, 2012
Decision	Substantially Equivalent
Regulation	874.4680

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View the full FDA submission: accessdata.fda.gov

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FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EB-530US

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