K-number	K051553
Device name	FUJI SYNAPSE WORKSTATION SOFTWARE
Applicant	Fujifilm Medical Systems U.S.A, Inc.
Product code	LLZ
Device class	Class II
Decision date	Jul 7, 2005
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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FUJI SYNAPSE WORKSTATION SOFTWARE

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