K-number	K170858
Device name	FDR AQRO (DR-XD 1000)
Applicant	Fujifilm Medical Systems U.S.A, Inc.
Product code	IZL
Device class	Class II
Decision date	Apr 24, 2017
Decision	Substantially Equivalent
Regulation	892.1720

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View the full FDA submission: accessdata.fda.gov

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FDR AQRO (DR-XD 1000)

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