K-number	K170451
Device name	FDX Console (DR-ID300CL) Software
Applicant	Fujifilm Medical Systems U.S.A, Inc.
Product code	LLZ
Device class	Class II
Decision date	Mar 16, 2017
Decision	Substantially Equivalent
Regulation	892.2050

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Source

View the full FDA submission: accessdata.fda.gov

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FDX Console (DR-ID300CL) Software

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